Variant report

Variant	nsv946401
Chromosome Location	chr1:153963837-153965429
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:0)
Chromatin interactive
region (count:60)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:153965256-153965748	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:153962873-153963867	H1-hESC	embryonic stem cell:	n/a	chr1:153963246-153963260
3	BCLAF1	chr1:153965191-153965737	GM12878	blood:	n/a	n/a
4	CEBPB	chr1:153963835-153964060	IMR90	lung:	n/a	n/a
5	CHD1	chr1:153962952-153964012	GM12878	blood:	n/a	n/a
6	CHD1	chr1:153962737-153964961	IMR90	lung:	n/a	n/a
7	CHD1	chr1:153963030-153964865	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr1:153965226-153965630	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr1:153965343-153965549	K562	blood:	n/a	n/a
10	ELF1	chr1:153964517-153964763	K562	blood:	n/a	n/a
11	GABPA	chr1:153962748-153963903	A549	lung:	n/a	chr1:153963225-153963232
12	GABPA	chr1:153962585-153964082	MCF-7	breast:	n/a	chr1:153963225-153963232
13	GATA2	chr1:153964347-153964651	HUVEC	blood vessel:	n/a	n/a
14	HCFC1	chr1:153962321-153964372	Hela-S3	cervix:	n/a	n/a
15	HEY1	chr1:153964445-153964722	HepG2	liver:	n/a	n/a
16	HEY1	chr1:153962912-153964190	HepG2	liver:	n/a	n/a
17	HEY1	chr1:153962967-153963871	K562	blood:	n/a	n/a
18	HEY1	chr1:153965377-153965657	K562	blood:	n/a	n/a
19	HEY1	chr1:153964294-153964714	K562	blood:	n/a	n/a
20	HEY1	chr1:153964968-153965661	K562	blood:	n/a	n/a
21	HEY1	chr1:153962970-153964244	K562	blood:	n/a	n/a
22	HEY1	chr1:153965126-153965789	HepG2	liver:	n/a	n/a
23	HEY1	chr1:153965100-153965818	HepG2	liver:	n/a	n/a
24	HEY1	chr1:153964358-153964811	HepG2	liver:	n/a	n/a
25	JUND	chr1:153962736-153964062	SK-N-SH	brain:	n/a	n/a
26	MAFF	chr1:153965154-153965654	K562	blood:	n/a	n/a
27	MAX	chr1:153962904-153963870	MCF-7	breast:	n/a	n/a
28	MAX	chr1:153962806-153963838	A549	lung:	n/a	n/a
29	MAZ	chr1:153962760-153964069	IMR90	lung:	n/a	n/a
30	MTA3	chr1:153965125-153965828	GM12878	blood:	n/a	n/a
31	MTA3	chr1:153965046-153965879	GM12878	blood:	n/a	n/a
32	MXI1	chr1:153965305-153965538	GM12878	blood:	n/a	n/a
33	MXI1	chr1:153962744-153964449	IMR90	lung:	n/a	n/a
34	MXI1	chr1:153965200-153965272	K562	blood:	n/a	n/a
35	MXI1	chr1:153962741-153964827	SK-N-SH	brain:	n/a	n/a
36	MYC	chr1:153962918-153964051	K562	blood:	n/a	n/a
37	MYC	chr1:153962924-153963868	K562	blood:	n/a	n/a
38	MYC	chr1:153963785-153963914	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr1:153962914-153963937	Raji	blood:	n/a	n/a
40	POLR2A	chr1:153964797-153965882	GM12891	blood:	n/a	n/a
41	POLR2A	chr1:153965099-153965700	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr1:153962895-153968418	K562	blood:	n/a	n/a
43	POLR2A	chr1:153965428-153965619	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr1:153963007-153964601	GM12891	blood:	n/a	n/a
45	POLR2A	chr1:153964793-153967747	HepG2	liver:	n/a	n/a
46	POLR2A	chr1:153962877-153968982	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr1:153962903-153964063	GM19099	blood:	n/a	n/a
48	POLR2A	chr1:153962725-153967624	PFSK-1	brain:	n/a	n/a
49	POLR2A	chr1:153964505-153964669	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr1:153965005-153965605	HCT-116	colon:	n/a	n/a

No data

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:153962867..153965202-chr1:154154379..154156785,3	MCF-7	breast:
2	chr1:153962343..153963954-chr1:154245938..154247539,2	K562	blood:
3	chr1:153605618..153608356-chr1:153961854..153964729,2	MCF-7	breast:
4	chr1:153964844..153966669-chr1:154089731..154091606,2	MCF-7	breast:
5	chr1:153512598..153514775-chr1:153963105..153964823,2	K562	blood:
6	chr1:153598208..153601029-chr1:153962097..153964477,2	K562	blood:
7	chr1:153962946..153964681-chr1:154191539..154193335,3	MCF-7	breast:
8	chr1:153917215..153920392-chr1:153961808..153965282,6	K562	blood:
9	chr1:153962483..153964703-chr1:154162511..154166249,3	MCF-7	breast:
10	chr1:153963961..153964489-chr17:19280358..19281310,2	Hela-S3	cervix:
11	chr1:153765340..153768610-chr1:153963132..153965319,3	K562	blood:
12	chr1:153771964..153774783-chr1:153963407..153965069,2	K562	blood:
13	chr1:153652530..153654579-chr1:153961932..153964850,2	K562	blood:
14	chr1:153962369..153964805-chr1:154243433..154246826,4	MCF-7	breast:
15	chr1:153699945..153701474-chr1:153962186..153964682,2	K562	blood:
16	chr1:153963924..153966450-chr1:154110406..154113402,2	K562	blood:
17	chr1:153964838..153965772-chr15:83876162..83876909,2	Hela-S3	cervix:
18	chr1:153745179..153749280-chr1:153961747..153968478,7	MCF-7	breast:
19	chr1:153603477..153606996-chr1:153962238..153964716,3	K562	blood:
20	chr1:43406457..43407090-chr1:153963456..153963963,2	Hela-S3	cervix:
21	chr1:153963387..153964006-chr15:65588101..65588979,2	Hela-S3	cervix:
22	chr1:153791929..153794477-chr1:153963416..153966079,2	K562	blood:
23	chr1:153905142..153906836-chr1:153961384..153963973,2	K562	blood:
24	chr1:153964000..153964634-chr5:150137543..150138443,2	Hela-S3	cervix:
25	chr1:153747289..153750894-chr1:153961895..153964874,3	MCF-7	breast:
26	chr1:153586138..153590435-chr1:153962533..153966036,4	K562	blood:
27	chr1:153961881..153966027-chr1:154151379..154156773,10	MCF-7	breast:
28	chr1:153961971..153964744-chr6:27100182..27102088,2	K562	blood:
29	chr1:153963252..153965177-chr1:154158511..154161067,3	MCF-7	breast:
30	chr1:70876781..70877378-chr1:153963481..153964310,2	Hela-S3	cervix:
31	chr1:153642259..153645171-chr1:153961754..153965588,6	K562	blood:
32	chr1:153537679..153540436-chr1:153962275..153964884,2	K562	blood:
33	chr1:153629459..153632821-chr1:153961630..153966753,5	K562	blood:
34	chr1:153961745..153965852-chr1:154153352..154156776,9	K562	blood:
35	chr1:153536925..153539179-chr1:153962275..153964605,2	K562	blood:
36	chr1:153963267..153965120-chr1:154971988..154974944,2	K562	blood:
37	chr1:153962189..153967020-chr1:154149779..154153923,7	MCF-7	breast:
38	chr1:153963264..153964008-chr11:45939253..45940040,2	Hela-S3	cervix:
39	chr1:153642202..153645171-chr1:153961721..153964784,6	K562	blood:
40	chr1:153962964..153963839-chr20:55203943..55204615,2	Hela-S3	cervix:
41	chr1:153961925..153965410-chr1:154146555..154149414,3	MCF-7	breast:
42	chr1:153965322..153967162-chr1:154193447..154195978,2	K562	blood:
43	chr1:153890756..153897034-chr1:153961597..153964863,14	K562	blood:
44	chr1:153961938..153967162-chr1:154189861..154195978,9	K562	blood:
45	chr1:153965120..153966091-chr18:12838469..12839213,2	Hela-S3	cervix:
46	chr1:153603477..153607903-chr1:153962238..153965498,5	K562	blood:
47	chr1:93810969..93811917-chr1:153965058..153965620,2	Hela-S3	cervix:
48	chr1:153963702..153965277-chr1:154515258..154516911,2	K562	blood:
49	chr1:153699974..153702840-chr1:153961694..153964834,3	K562	blood:
50	chr1:153961855..153964878-chr1:154149314..154153044,5	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPS27-2	chr1:153964682-153964721	NONHSAT006576

No data

Variant related genes	Relation type
ENSG00000231416	TF binding region
ENSG00000272030	chromatin interactions
ENSG00000143545	chromatin interactions
ENSG00000160678	chromatin interactions
ENSG00000117505	chromatin interactions
ENSG00000169418	chromatin interactions
ENSG00000198837	chromatin interactions
ENSG00000223745	chromatin interactions
ENSG00000231827	chromatin interactions
ENSG00000143614	chromatin interactions
ENSG00000121680	chromatin interactions
ENSG00000087510	chromatin interactions
ENSG00000143612	chromatin interactions
ENSG00000132912	chromatin interactions
ENSG00000166484	chromatin interactions
ENSG00000108641	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000143554	chromatin interactions
ENSG00000166503	chromatin interactions
ENSG00000189171	chromatin interactions
ENSG00000207039	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000143624	chromatin interactions
ENSG00000189334	chromatin interactions
ENSG00000271853	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000215938	chromatin interactions
ENSG00000143553	chromatin interactions
ENSG00000143575	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000143621	chromatin interactions
ENSG00000160679	chromatin interactions
ENSG00000196420	chromatin interactions
ENSG00000196754	chromatin interactions
ENSG00000143569	chromatin interactions
ENSG00000143549	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138107939	chr1:153963838-153963839	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	31 gene(s)	Overlapped CNVs	n/a
2	rs73010768	chr1:153963878-153963879	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
3	rs545487843	chr1:153963917-153963918	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
4	rs536075603	chr1:153963926-153963927	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
5	rs114120114	chr1:153963983-153963984	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	31 gene(s)	Overlapped CNVs	n/a
6	rs2633	chr1:153963990-153963991	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	31 gene(s)	Overlapped CNVs	n/a
7	rs140257179	chr1:153963995-153963996	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	31 gene(s)	Overlapped CNVs	n/a
8	rs35506293	chr1:153963996-153963997	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	31 gene(s)	Overlapped CNVs	n/a
9	rs397713349	chr1:153963998-153963999	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	31 gene(s)	Overlapped CNVs	n/a
10	rs147042648	chr1:153964016-153964017	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
11	rs2632	chr1:153964021-153964022	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
12	rs367550840	chr1:153964026-153964027	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
13	rs371349094	chr1:153964034-153964035	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
14	rs372202101	chr1:153964064-153964065	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
15	rs150298203	chr1:153964067-153964068	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
16	rs549879404	chr1:153964115-153964116	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
17	rs567792813	chr1:153964165-153964166	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
18	rs375509510	chr1:153964170-153964171	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
19	rs370162121	chr1:153964206-153964207	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
20	rs56042740	chr1:153964223-153964224	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
21	rs180990585	chr1:153964240-153964241	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
22	rs565645368	chr1:153964250-153964251	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
23	rs539301175	chr1:153964252-153964253	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
24	rs557887486	chr1:153964308-153964309	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
25	rs570066643	chr1:153964319-153964320	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
26	rs185823301	chr1:153964330-153964331	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
27	rs555878293	chr1:153964332-153964333	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
28	rs113108816	chr1:153964377-153964378	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
29	rs574172480	chr1:153964388-153964389	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
30	rs200838458	chr1:153964396-153964397	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
31	rs397693735	chr1:153964397-153964398	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
32	rs575235151	chr1:153964410-153964411	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
33	rs146915876	chr1:153964418-153964419	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
34	rs143906786	chr1:153964455-153964456	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
35	rs192335762	chr1:153964467-153964468	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
36	rs545646722	chr1:153964469-153964470	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
37	rs371744802	chr1:153964473-153964474	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
38	rs374937935	chr1:153964474-153964475	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
39	rs563810268	chr1:153964493-153964494	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
40	rs369917516	chr1:153964499-153964500	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
41	rs376089458	chr1:153964507-153964508	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
42	rs181933252	chr1:153964512-153964513	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
43	rs138950537	chr1:153964542-153964543	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
44	rs138711692	chr1:153964550-153964551	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
45	rs561486197	chr1:153964563-153964564	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
46	rs376220786	chr1:153964593-153964594	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
47	rs528913644	chr1:153964605-153964606	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
48	rs376914690	chr1:153964618-153964619	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
49	rs547192169	chr1:153964698-153964699	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	25 gene(s)	Overlapped CNVs	n/a
50	rs370663668	chr1:153964722-153964723	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Liver carcinoma	19366792	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153962600-153964000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:153962600-153964000	Active TSS	Brain Anterior Caudate	brain
3	chr1:153962600-153964000	Active TSS	Stomach Smooth Muscle	stomach
4	chr1:153962800-153964000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:153962800-153964000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:153962800-153964000	Active TSS	Brain Cingulate Gyrus	brain
7	chr1:153962800-153964000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:153962800-153964000	Active TSS	Duodenum Smooth Muscle	Duodenum
9	chr1:153962800-153964000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
10	chr1:153962800-153964000	Active TSS	Fetal Brain Female	brain
11	chr1:153962800-153964000	Active TSS	Fetal Intestine Large	intestine
12	chr1:153962800-153964000	Active TSS	Fetal Lung	lung
13	chr1:153962800-153964000	Active TSS	Fetal Muscle Trunk	muscle
14	chr1:153962800-153964000	Active TSS	Fetal Muscle Leg	muscle
15	chr1:153962800-153964000	Active TSS	Fetal Stomach	stomach
16	chr1:153962800-153964000	Active TSS	Thymus	Thymus
17	chr1:153962800-153964000	Active TSS	NH-A	brain
18	chr1:153962800-153964000	Active TSS	NHDF-Ad	bronchial
19	chr1:153962800-153964200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:153962800-153964200	Active TSS	Aorta	Aorta
21	chr1:153962800-153964200	Active TSS	Brain Hippocampus Middle	brain
22	chr1:153962800-153964200	Active TSS	HSMMtube	muscle
23	chr1:153962800-153964400	Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr1:153962800-153964400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:153962800-153964400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:153962800-153964400	Active TSS	Fetal Intestine Small	intestine
27	chr1:153962800-153964400	Active TSS	Left Ventricle	heart
28	chr1:153962800-153964400	Active TSS	Ovary	ovary
29	chr1:153962800-153964400	Active TSS	Psoas Muscle	Psoas
30	chr1:153962800-153964600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr1:153962800-153965200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:153962800-153965600	Active TSS	Right Atrium	heart
33	chr1:153963000-153964000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr1:153963000-153964000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr1:153963000-153964000	Active TSS	Primary T cells fromperipheralblood	blood
36	chr1:153963000-153964000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr1:153963000-153964000	Active TSS	Brain Angular Gyrus	brain
38	chr1:153963000-153964000	Active TSS	Esophagus	oesophagus
39	chr1:153963000-153964000	Active TSS	Placenta	Placenta
40	chr1:153963000-153964000	Active TSS	Rectal Mucosa Donor 31	rectum
41	chr1:153963000-153964200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr1:153963000-153964200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr1:153963000-153964200	Active TSS	Fetal Kidney	kidney
44	chr1:153963000-153964200	Active TSS	GM12878-XiMat	blood
45	chr1:153963000-153964400	Active TSS	H9 Cell Line	embryonic stem cell
46	chr1:153963000-153964400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr1:153963200-153964000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:153963200-153964000	Active TSS	Placenta Amnion	Placenta Amnion
49	chr1:153963200-153964000	Active TSS	Sigmoid Colon	Sigmoid Colon
50	chr1:153963200-153964000	Active TSS	Small Intestine	intestine

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