Variant report

Variant	esv1803652
Chromosome Location	chr7:38372659-38407572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2074)
CpG islands
(count:610)
Chromatin interactive
region (count:23)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2074 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38375261-38375775	K562	blood:	n/a	n/a
2	ARID3A	chr7:38380924-38381236	K562	blood:	n/a	n/a
3	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
4	ATF1	chr7:38375268-38375593	K562	blood:	n/a	n/a
5	ATF1	chr7:38380742-38381291	K562	blood:	n/a	n/a
6	ATF1	chr7:38375958-38376139	K562	blood:	n/a	n/a
7	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
8	ATF2	chr7:38375154-38375534	GM12878	blood:	n/a	n/a
9	ATF2	chr7:38375126-38375565	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:38375250-38375572	K562	blood:	n/a	n/a
11	ATF3	chr7:38375159-38375625	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:38375296-38375468	K562	blood:	n/a	n/a
13	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
14	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
15	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
16	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
17	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
18	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
19	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
20	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
21	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
22	BATF	chr7:38375071-38375552	GM12878	blood:	n/a	n/a
23	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
24	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
25	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
26	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
27	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
28	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
29	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
31	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
33	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
34	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
35	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
36	BCL3	chr7:38375082-38375686	A549	lung:	n/a	chr7:38375198-38375207
37	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
38	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
39	BCLAF1	chr7:38375138-38375654	GM12878	blood:	n/a	chr7:38375198-38375207
40	BCLAF1	chr7:38375115-38375667	GM12878	blood:	n/a	chr7:38375198-38375207
41	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a
45	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
46	BHLHE40	chr7:38375174-38375547	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
48	BHLHE40	chr7:38374979-38376051	K562	blood:	n/a	n/a
49	BHLHE40	chr7:38380767-38381281	K562	blood:	n/a	n/a
50	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38389991-38390041	NB4	blood:	n/a
2	chr7:38398839-38398889	AG10803	skin:	n/a
3	chr7:38398839-38398889	ovcar-3	ovarian:	n/a
4	chr7:38389991-38390041	A549	lung:	n/a
5	chr7:38389991-38390041	H1-hESC	embryonic stem cell:	embryo
6	chr7:38375376-38375426	U87	brain:	n/a
7	chr7:38398839-38398889	HRCEpiC	kidney:	n/a
8	chr7:38375485-38375535	LNCaP	prostate:	n/a
9	chr7:38389685-38389735	BE2_C	brain:	n/a
10	chr7:38398836-38398886	GM06990	blood:	n/a
11	chr7:38398839-38398889	A549	lung:	n/a
12	chr7:38380487-38380537	U87	brain:	n/a
13	chr7:38380487-38380537	SK-N-SH_RA	brain:	n/a
14	chr7:38389991-38390041	PrEC	prostate:	n/a
15	chr7:38380582-38380632	NT2-D1	testis:	n/a
16	chr7:38375485-38375535	HEK293	kidney:	embryo
17	chr7:38375485-38375535	IMR90	lung:	fetal
18	chr7:38380487-38380537	HUVEC	blood vessel:	n/a
19	chr7:38380487-38380537	NT2-D1	testis:	n/a
20	chr7:38389659-38389709	AG09309	skin:	n/a
21	chr7:38403507-38403557	A549	lung:	n/a
22	chr7:38380487-38380537	AG04449	skin:	fetal
23	chr7:38389659-38389709	HIPEpiC	eye:	n/a
24	chr7:38380582-38380632	K562	blood:	n/a
25	chr7:38389685-38389735	BJ	skin:	n/a
26	chr7:38375485-38375535	Jurkat	blood:	n/a
27	chr7:38389991-38390041	GM06990	blood:	n/a
28	chr7:38375485-38375535	SK-N-SH	brain:	n/a
29	chr7:38389991-38390041	GM12878	blood:	n/a
30	chr7:38375485-38375535	MCF-7	breast:	n/a
31	chr7:38389685-38389735	SKMC	muscle:	n/a
32	chr7:38398839-38398889	Jurkat	blood:	n/a
33	chr7:38380582-38380632	BJ	skin:	n/a
34	chr7:38403507-38403557	Hepatocyte	liver:	n/a
35	chr7:38389659-38389709	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:38380487-38380537	NHDF-neo	bronchial:	n/a
37	chr7:38380487-38380537	HL-60	blood:	n/a
38	chr7:38398836-38398886	MCF10A-Er-Src	breast:	n/a
39	chr7:38375485-38375535	HCPEpiC	choroid plexus:	n/a
40	chr7:38380487-38380537	SAEC	small airway:	n/a
41	chr7:38389685-38389735	HCF	heart:	n/a
42	chr7:38398836-38398886	HRE	kidney:	n/a
43	chr7:38389991-38390041	HEEpiC	esophagus:	n/a
44	chr7:38389991-38390041	HAEpiC	amniotic membrane:	n/a
45	chr7:38389659-38389709	GM12878	blood:	n/a
46	chr7:38380582-38380632	Caco-2	colon:	n/a
47	chr7:38380582-38380632	PrEC	prostate:	n/a
48	chr7:38389685-38389735	ovcar-3	ovarian:	n/a
49	chr7:38380487-38380537	HAEpiC	amniotic membrane:	n/a
50	chr7:38403507-38403557	PrEC	prostate:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
2	chr7:38369664..38372472-chr7:38373590..38376789,3	K562	blood:
3	chr7:38350491..38353138-chr7:38373860..38375500,2	K562	blood:
4	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
5	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
6	chr7:38350441..38353889-chr7:38368470..38373744,5	K562	blood:
7	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
8	chr7:38255022..38255645-chr7:38375302..38376120,3	MCF-7	breast:
9	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
10	chr7:38350491..38352001-chr7:38373860..38376555,2	K562	blood:
11	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
12	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
13	chr7:38269978..38272526-chr7:38377435..38379545,2	K562	blood:
14	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
15	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
16	chr7:38380741..38382401-chr7:38383649..38386131,2	K562	blood:
17	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
18	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
19	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
20	chr7:38375472..38376033-chr7:38384935..38385704,2	MCF-7	breast:
21	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
22	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
23	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
2	lnc-STARD3NL-1	chr7:38381216-38381400	ENSG00000250924
3	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
4	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1
5	lnc-STARD3NL-1	chr7:38381098-38381400	NONHSAT120178
6	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
7	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
8	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
9	lnc-STARD3NL-1	chr7:38381747-38382154	NONHSAT120178
10	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
11	lnc-AMPH-5	chr7:38375073-38375115	NONHSAT120177
12	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
13	lnc-AMPH-5	chr7:38374642-38374951	NONHSAT120177
14	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
15	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
16	lnc-STARD3NL-1	chr7:38381178-38381400	NONHSAT120179
17	lnc-AMPH-1	chr7:38407246-38407494	XLOC_006412
18	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
19	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182

No data

Variant related genes	Relation type
TRGV2	TF binding region
ENSG00000272908	TF binding region
TRGV7	TF binding region
TRGV5	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV8	TF binding region
TRGV5P	TF binding region
TRGV2	CpG island
ENSG00000272908	CpG island
TRGV7	CpG island
TRGV5	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV8	CpG island
TRGV5P	CpG island
ENSG00000211696	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000211698	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000249978	chromatin interactions
RAB5A	miRNA target sites
CA13	miRNA target sites
SERTAD3	miRNA target sites

Extended variants
information (count: 2130 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2130 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567590105	chr7:38372663-38372664	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs536669545	chr7:38372664-38372665	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs117123736	chr7:38372696-38372697	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs139890593	chr7:38372701-38372702	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs538836000	chr7:38372704-38372705	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs143114462	chr7:38372719-38372720	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs574973355	chr7:38372722-38372723	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs146667989	chr7:38372726-38372727	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs184895719	chr7:38372727-38372728	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs189755289	chr7:38372746-38372747	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs9639790	chr7:38372818-38372819	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs115441109	chr7:38372846-38372847	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs569510355	chr7:38372857-38372858	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs9639791	chr7:38372869-38372870	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs570076741	chr7:38372917-38372918	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs192708884	chr7:38372929-38372930	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs372137612	chr7:38372950-38372951	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs62444997	chr7:38372967-38372968	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs375564586	chr7:38373023-38373024	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs78293521	chr7:38373045-38373046	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs140373785	chr7:38373054-38373055	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs9639792	chr7:38373216-38373217	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs566819735	chr7:38373218-38373219	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs372551102	chr7:38373320-38373321	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs538974642	chr7:38373330-38373331	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs148502038	chr7:38373333-38373334	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs576948207	chr7:38373334-38373335	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs149952079	chr7:38373418-38373419	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs35805030	chr7:38373422-38373423	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200105509	chr7:38373493-38373494	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs34215527	chr7:38373496-38373497	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs575398608	chr7:38373502-38373503	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184466665	chr7:38373524-38373525	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs2534578	chr7:38373531-38373532	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs79536549	chr7:38373572-38373573	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145128594	chr7:38373574-38373575	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539838239	chr7:38373586-38373587	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs77864487	chr7:38373587-38373588	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs544691533	chr7:38373712-38373713	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs181974109	chr7:38373725-38373726	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs562902455	chr7:38373737-38373738	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs2735164	chr7:38373761-38373762	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
43	rs185992335	chr7:38373797-38373798	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs2735163	chr7:38373828-38373829	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561214162	chr7:38373844-38373845	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs530257630	chr7:38373851-38373852	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs62444998	chr7:38373860-38373861	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs9785016	chr7:38373879-38373880	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs2735162	chr7:38373887-38373888	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs149083432	chr7:38373892-38373893	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38366800-38375200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr7:38369200-38375400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:38369800-38373800	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
4	chr7:38370200-38373800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr7:38370200-38373800	Enhancers	Dnd41	blood
6	chr7:38370200-38374000	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr7:38370400-38374800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr7:38370800-38372800	Enhancers	Fetal Intestine Large	intestine
9	chr7:38370800-38374200	Weak transcription	Placenta	Placenta
10	chr7:38371000-38374400	Weak transcription	Adipose Nuclei	Adipose
11	chr7:38371000-38374400	Weak transcription	Fetal Muscle Leg	muscle
12	chr7:38371000-38375200	Weak transcription	Primary T cells from cord blood	blood
13	chr7:38371000-38375200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr7:38371000-38375400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:38371000-38375400	Weak transcription	Lung	lung
16	chr7:38371200-38374200	Weak transcription	Thymus	Thymus
17	chr7:38371200-38374600	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr7:38371200-38375200	Active TSS	Primary T cells fromperipheralblood	blood
19	chr7:38371600-38374800	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr7:38371600-38375200	Weak transcription	A549	lung
21	chr7:38371800-38372800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr7:38371800-38373800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:38371800-38380600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:38372000-38372800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr7:38372000-38374200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:38372000-38374400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr7:38372000-38374800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr7:38372000-38375000	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr7:38372200-38374200	Weak transcription	Fetal Thymus	thymus
30	chr7:38372400-38373400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
31	chr7:38372600-38372800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:38372600-38373000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
33	chr7:38372600-38373000	Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chr7:38372600-38374200	Weak transcription	K562	blood
35	chr7:38372800-38373000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:38372800-38373000	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr7:38372800-38373600	Active TSS	Primary B cells from cord blood	blood
38	chr7:38372800-38374200	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr7:38372800-38374400	Weak transcription	Fetal Intestine Large	intestine
40	chr7:38372800-38375000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:38373000-38374200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr7:38373000-38374400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr7:38373000-38374800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr7:38373400-38373800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr7:38373400-38375400	Weak transcription	Gastric	stomach
46	chr7:38373600-38374400	Weak transcription	Primary B cells from cord blood	blood
47	chr7:38373800-38374200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:38373800-38374200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr7:38373800-38374600	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr7:38373800-38374600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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