Variant report

Variant	nsv1024586
Chromosome Location	chr7:8243829-8490078
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3397)
CpG islands
(count:4215)
Chromatin interactive
region (count:209)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3397 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:8458315-8458652	K562	blood:	n/a	n/a
2	ARID3A	chr7:8272380-8273332	K562	blood:	n/a	n/a
3	ARID3A	chr7:8430964-8431383	K562	blood:	n/a	n/a
4	ARID3A	chr7:8317118-8317430	K562	blood:	n/a	n/a
5	ARID3A	chr7:8426612-8427180	K562	blood:	n/a	n/a
6	ARID3A	chr7:8255604-8255776	K562	blood:	n/a	n/a
7	ARID3A	chr7:8335603-8336008	K562	blood:	n/a	n/a
8	ARID3A	chr7:8343584-8343742	K562	blood:	n/a	n/a
9	ARID3A	chr7:8257133-8257487	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:8364734-8364927	K562	blood:	n/a	n/a
11	ARID3A	chr7:8335663-8336040	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:8257120-8257547	K562	blood:	n/a	n/a
13	ARID3A	chr7:8476565-8476764	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:8301790-8301845	K562	blood:	n/a	n/a
15	ARID3A	chr7:8300420-8300901	K562	blood:	n/a	n/a
16	ARID3A	chr7:8458395-8458679	HepG2	liver:	n/a	n/a
17	ATF1	chr7:8335718-8336040	K562	blood:	n/a	n/a
18	ATF1	chr7:8257101-8257328	K562	blood:	n/a	n/a
19	ATF1	chr7:8297739-8298066	K562	blood:	n/a	n/a
20	ATF1	chr7:8260230-8260335	K562	blood:	n/a	n/a
21	ATF1	chr7:8330353-8330861	K562	blood:	n/a	n/a
22	ATF1	chr7:8426594-8427186	K562	blood:	n/a	n/a
23	ATF1	chr7:8431081-8431383	K562	blood:	n/a	n/a
24	ATF1	chr7:8272553-8272941	K562	blood:	n/a	n/a
25	ATF2	chr7:8426425-8427384	GM12878	blood:	n/a	n/a
26	ATF2	chr7:8426657-8427138	GM12878	blood:	n/a	n/a
27	ATF3	chr7:8330598-8330811	K562	blood:	n/a	n/a
28	ATF3	chr7:8343611-8343854	K562	blood:	n/a	n/a
29	ATF3	chr7:8482710-8483002	H1-hESC	embryonic stem cell:	n/a	chr7:8482881-8482890
30	ATF3	chr7:8426727-8427084	K562	blood:	n/a	n/a
31	ATF3	chr7:8482695-8483062	H1-hESC	embryonic stem cell:	n/a	chr7:8482881-8482890
32	ATF3	chr7:8272514-8273020	K562	blood:	n/a	n/a
33	BACH1	chr7:8473178-8474204	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr7:8474714-8474795	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr7:8466543-8466583	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr7:8285895-8286015	K562	blood:	n/a	n/a
37	BACH1	chr7:8336305-8336447	K562	blood:	n/a	n/a
38	BACH1	chr7:8290259-8290459	K562	blood:	n/a	n/a
39	BACH1	chr7:8476689-8476861	K562	blood:	n/a	n/a
40	BACH1	chr7:8482352-8482931	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr7:8364354-8364374	K562	blood:	n/a	n/a
42	BATF	chr7:8426653-8427043	GM12878	blood:	n/a	chr7:8426897-8426907 chr7:8426896-8426907
43	BATF	chr7:8426669-8427077	GM12878	blood:	n/a	chr7:8426897-8426907 chr7:8426896-8426907
44	BCL11A	chr7:8405176-8405398	H1-hESC	embryonic stem cell:	n/a	n/a
45	BCLAF1	chr7:8272453-8272925	K562	blood:	n/a	n/a
46	BHLHE40	chr7:8300597-8301032	K562	blood:	n/a	n/a
47	BHLHE40	chr7:8270858-8270944	K562	blood:	n/a	n/a
48	BHLHE40	chr7:8473169-8473622	HepG2	liver:	n/a	n/a
49	BHLHE40	chr7:8343540-8344243	K562	blood:	n/a	n/a
50	BHLHE40	chr7:8473533-8473815	K562	blood:	n/a	n/a

(count:4215 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:8276021-8276071	NHBE	bronchial:	n/a
2	chr7:8486611-8486661	MCF10A-Er-Src	breast:	n/a
3	chr7:8481036-8481086	HCPEpiC	choroid plexus:	n/a
4	chr7:8304543-8304593	AG04449	skin:	fetal
5	chr7:8476128-8476178	CMK	blood:	n/a
6	chr7:8276021-8276071	Hepatocyte	liver:	n/a
7	chr7:8276021-8276071	NHBE	bronchial:	n/a
8	chr7:8486611-8486661	MCF10A-Er-Src	breast:	n/a
9	chr7:8481036-8481086	HCPEpiC	choroid plexus:	n/a
10	chr7:8304543-8304593	AG04449	skin:	fetal
11	chr7:8476128-8476178	CMK	blood:	n/a
12	chr7:8276021-8276071	Hepatocyte	liver:	n/a
13	chr7:8477029-8477079	HL-60	blood:	n/a
14	chr7:8302271-8302321	U87	brain:	n/a
15	chr7:8473385-8473435	GM12891	blood:	n/a
16	chr7:8476450-8476500	GM06990	blood:	n/a
17	chr7:8304543-8304593	GM06990	blood:	n/a
18	chr7:8473234-8473284	AoSMC	blood vessel:	n/a
19	chr7:8481036-8481086	H1-hESC	embryonic stem cell:	embryo
20	chr7:8300728-8300778	PANC-1	pancreas:	n/a
21	chr7:8480779-8480829	GM19239	blood:	n/a
22	chr7:8482877-8482927	ECC-1	luminal epithelium:	n/a
23	chr7:8343477-8343527	K562	blood:	n/a
24	chr7:8481537-8481587	Hepatocyte	liver:	n/a
25	chr7:8383869-8383919	Jurkat	blood:	n/a
26	chr7:8473385-8473435	GM06990	blood:	n/a
27	chr7:8482614-8482664	AoSMC	blood vessel:	n/a
28	chr7:8476098-8476148	PFSK-1	brain:	n/a
29	chr7:8261154-8261204	SK-N-MC	brain:	n/a
30	chr7:8476730-8476780	MCF-7	breast:	n/a
31	chr7:8429907-8429957	HMEC	breast:	n/a
32	chr7:8476098-8476148	RPTEC	kidney:	n/a
33	chr7:8302271-8302321	GM12878	blood:	n/a
34	chr7:8343477-8343527	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:8477156-8477206	BE2_C	brain:	n/a
36	chr7:8276812-8276862	CMK	blood:	n/a
37	chr7:8302731-8302781	AG04449	skin:	fetal
38	chr7:8473279-8473329	HepG2	liver:	n/a
39	chr7:8302251-8302301	SKMC	muscle:	n/a
40	chr7:8302191-8302241	NH-A	brain:	n/a
41	chr7:8482235-8482285	NB4	blood:	n/a
42	chr7:8277690-8277740	ProgFib	skin:	n/a
43	chr7:8473279-8473329	SK-N-SH_RA	brain:	n/a
44	chr7:8476128-8476178	RPTEC	kidney:	n/a
45	chr7:8300728-8300778	H1-hESC	embryonic stem cell:	embryo
46	chr7:8483374-8483424	GM12892	blood:	n/a
47	chr7:8301435-8301485	HCPEpiC	choroid plexus:	n/a
48	chr7:8477597-8477647	IMR90	lung:	fetal
49	chr7:8483249-8483299	SK-N-MC	brain:	n/a
50	chr7:8483569-8483619	IMR90	lung:	fetal

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:8306577..8308264-chr7:8324025..8326731,2	K562	blood:
2	chr7:8395934..8398009-chr7:8409383..8411408,2	MCF-7	breast:
3	chr7:8365461..8367052-chr7:8371679..8374090,2	MCF-7	breast:
4	chr7:8255292..8257322-chr7:8259822..8262146,2	K562	blood:
5	chr7:8346660..8349456-chr7:8350822..8352856,2	K562	blood:
6	chr7:8425326..8427530-chr7:8427917..8429506,2	MCF-7	breast:
7	chr7:8299444..8303405-chr7:8332174..8336347,8	MCF-7	breast:
8	chr7:8293106..8296344-chr7:8297870..8301843,5	K562	blood:
9	chr7:8476110..8477803-chr7:8763425..8764387,8	MCF-7	breast:
10	chr7:8457706..8459634-chr7:8470268..8471926,2	MCF-7	breast:
11	chr7:7601559..7604327-chr7:8300528..8302351,2	MCF-7	breast:
12	chr7:8268538..8270309-chr7:8271009..8273384,2	K562	blood:
13	chr7:8346660..8349456-chr7:8350822..8352856,2	K562	blood:
14	chr7:8335652..8336362-chr7:8404897..8405424,2	MCF-7	breast:
15	chr7:8306995..8310777-chr7:8311196..8314720,3	K562	blood:
16	chr7:7678479..7681346-chr7:8300009..8302111,2	K562	blood:
17	chr7:8322298..8327046-chr7:8329175..8332951,4	MCF-7	breast:
18	chr7:8314102..8315802-chr7:8320914..8322938,2	MCF-7	breast:
19	chr14:59950994..59951855-chr7:8301396..8302024,2	HCT-116	colon:
20	chr7:8259010..8260776-chr7:8333420..8335671,2	MCF-7	breast:
21	chr7:8227287..8229114-chr7:8244454..8246101,2	K562	blood:
22	chr7:8393598..8396534-chr7:8400388..8402871,3	MCF-7	breast:
23	chr7:8372140..8374996-chr7:8377219..8379253,2	MCF-7	breast:
24	chr7:8284762..8287625-chr7:8298919..8300747,2	MCF-7	breast:
25	chr7:8257061..8257622-chr7:8334918..8335755,2	MCF-7	breast:
26	chr7:8353412..8355160-chr7:8364967..8367694,2	MCF-7	breast:
27	chr7:8297158..8299148-chr7:8314480..8317301,2	K562	blood:
28	chr7:8404670..8406317-chr7:8430221..8432474,2	K562	blood:
29	chr7:8257061..8257622-chr7:8334918..8335755,2	MCF-7	breast:
30	chr7:8393598..8396534-chr7:8400388..8402871,3	MCF-7	breast:
31	chr7:8257240..8257766-chr7:8404862..8405637,2	MCF-7	breast:
32	chr7:8342220..8346219-chr7:8348386..8352683,4	K562	blood:
33	chr7:8271341..8275510-chr7:8300649..8303958,6	K562	blood:
34	chr7:8269043..8270724-chr7:8273457..8275087,2	K562	blood:
35	chr7:8381608..8383646-chr7:8392163..8393993,2	K562	blood:
36	chr7:8425326..8427530-chr7:8427917..8429506,2	MCF-7	breast:
37	chr17:56708762..56709669-chr7:8301587..8302120,2	HCT-116	colon:
38	chr7:8363447..8366490-chr7:8366907..8369516,4	K562	blood:
39	chr7:7680697..7682834-chr7:8264362..8267648,3	K562	blood:
40	chr7:8363447..8366490-chr7:8366907..8369516,4	K562	blood:
41	chr7:8476230..8477429-chr7:8763427..8764475,19	MCF-7	breast:
42	chr7:8458212..8458907-chr7:10747962..10748515,2	MCF-7	breast:
43	chr7:8353412..8355160-chr7:8364967..8367694,2	MCF-7	breast:
44	chr7:8471139..8473117-chr7:8475215..8477243,2	K562	blood:
45	chr7:8255292..8257322-chr7:8259822..8262146,2	K562	blood:
46	chr7:8305205..8307579-chr7:8319698..8322202,2	MCF-7	breast:
47	chr7:8271324..8275150-chr7:8300079..8303958,8	K562	blood:
48	chr7:8395934..8398009-chr7:8409383..8411408,2	MCF-7	breast:
49	chr7:8256019..8257810-chr7:8296899..8299475,2	MCF-7	breast:
50	chr16:18812683..18814346-chr7:8299005..8301772,2	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ICA1-4	chr7:8383337-8384124	NONHSAT119157
2	lnc-NXPH1-4	chr7:8346538-8346711	ucscGeneNc_uc003srt_1
3	lnc-GLCCI1-2	chr7:8302210-8302456	ENSG00000229970
4	lnc-RPA3-7	chr7:8258234-8258581	NONHSAT119153
5	lnc-GLCCI1-2	chr7:8302244-8302466	NONHSAT119155
6	lnc-GLCCI1-2	chr7:8380013-8380186	ENSG00000229970
7	lnc-RPA3-7	chr7:8258071-8258133	NONHSAT119153
8	lnc-NXPH1-2	chr7:8384553-8387652	NONHSAT119158
9	lnc-GLCCI1-2	chr7:8380647-8380973	ENSG00000229970
10	lnc-NXPH1-4	chr7:8268419-8268574	ucscGeneNc_uc003srt_1
11	lnc-GLCCI1-2	chr7:8301894-8302049	ENSG00000229970
12	lnc-GLCCI1-2	chr7:8383337-8384146	ENSG00000229970
13	lnc-GLCCI1-2	chr7:8302210-8302451	ENSG00000244239
14	lnc-ICA1-4	chr7:8382797-8382916	NONHSAT119157
15	lnc-GLCCI1-2	chr7:8382755-8382920	ENSG00000229970
16	lnc-ICA1-4	chr7:8393976-8394033	NONHSAT119157
17	lnc-NXPH1-4	chr7:8347172-8347381	ucscGeneNc_uc003srt_1
18	lnc-NXPH1-4	chr7:8349862-8350671	ucscGeneNc_uc003srt_1
19	lnc-NXPH1-4	chr7:8268735-8268981	ucscGeneNc_uc003srt_1
20	lnc-GLCCI1-2	chr7:8301863-8302049	ENSG00000244239
21	lnc-GLCCI1-2	chr7:8380647-8380856	ENSG00000229970
22	lnc-NXPH1-4	chr7:8270746-8270835	ucscGeneNc_uc003srt_1
23	lnc-GLCCI1-2	chr7:8304221-8304310	ENSG00000229970
24	lnc-GLCCI1-2	chr7:8302562-8302939	NONHSAT119155
25	lnc-GLCCI1-2	chr7:8343371-8343426	ENSG00000229970
26	lnc-NXPH1-4	chr7:8349280-8349445	ucscGeneNc_uc003srt_1
27	lnc-GLCCI1-2	chr7:8380013-8380186	ENSG00000229970

No data

Variant related genes	Relation type
ENSG00000244239	TF binding region
ENSG00000272328	TF binding region
NXPH1	TF binding region
ICA1	TF binding region
ENSG00000229970	TF binding region
ENSG00000244239	CpG island
ENSG00000272328	CpG island
NXPH1	CpG island
ICA1	CpG island
ENSG00000229970	CpG island
ENSG00000170540	chromatin interactions
ENSG00000219545	chromatin interactions
ENSG00000272328	chromatin interactions
ENSG00000244239	chromatin interactions
ENSG00000003147	chromatin interactions
ENSG00000229970	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000126790	chromatin interactions
ENSG00000153363	chromatin interactions
ENSG00000106399	chromatin interactions
ENSG00000233108	chromatin interactions
ENSG00000106415	chromatin interactions
ENSG00000260342	chromatin interactions
ENSG00000272894	chromatin interactions
ENSG00000164654	chromatin interactions
ENSG00000050130	chromatin interactions
ENSG00000171960	chromatin interactions
SSFA2	miRNA target sites
ERBB2IP	miRNA target sites
KLHDC5	miRNA target sites
SMARCC1	miRNA target sites
ARFIP1	miRNA target sites
ZSCAN12	miRNA target sites
SYBU	miRNA target sites
BCAT1	miRNA target sites
NVL	miRNA target sites

Extended variants
information (count: 9507 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:9507 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532193177	chr7:8243846-8243847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550323372	chr7:8243853-8243854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553522891	chr7:8243861-8243862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17144906	chr7:8243866-8243867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537599834	chr7:8243928-8243929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549200415	chr7:8243944-8243945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148097902	chr7:8243948-8243949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74611659	chr7:8243970-8243971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115792710	chr7:8243974-8243975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571934662	chr7:8243997-8243998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10952097	chr7:8244012-8244013	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs34459787	chr7:8244027-8244028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557542440	chr7:8244046-8244047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571795222	chr7:8244069-8244070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575903061	chr7:8244070-8244071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12670131	chr7:8244108-8244109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs141838201	chr7:8244127-8244128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79142582	chr7:8244169-8244170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539815518	chr7:8244205-8244206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564847484	chr7:8244227-8244228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569293652	chr7:8244282-8244283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532229173	chr7:8244310-8244311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544100182	chr7:8244346-8244347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562384399	chr7:8244354-8244355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs16872835	chr7:8244358-8244359	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188099280	chr7:8244381-8244382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567627892	chr7:8244407-8244408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4725076	chr7:8244409-8244410	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs180894655	chr7:8244412-8244413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186367751	chr7:8244415-8244416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139784674	chr7:8244430-8244431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375393606	chr7:8244452-8244453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571699903	chr7:8244456-8244457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557675177	chr7:8244531-8244532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144685554	chr7:8244571-8244572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571018199	chr7:8244577-8244578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147410080	chr7:8244578-8244579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554666985	chr7:8244608-8244609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139639656	chr7:8244635-8244636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540228814	chr7:8244636-8244637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558179293	chr7:8244697-8244698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576420840	chr7:8244704-8244705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs56223249	chr7:8244709-8244710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs398003587	chr7:8244724-8244725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376645177	chr7:8244728-8244729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs59171473	chr7:8244730-8244731	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs375933270	chr7:8244793-8244794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562421415	chr7:8244816-8244817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529922381	chr7:8244841-8244842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191274079	chr7:8244903-8244904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Williams Syndrome	20824207	CNVD
Renal cell carcinoma	18194544	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Depressive disorder	21152026	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22737080	CNVD

Chromatin state (count:2292 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:8216400-8247200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:8217600-8254800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:8225000-8245800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:8230400-8246200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:8230400-8246800	Weak transcription	Brain Germinal Matrix	brain
6	chr7:8230600-8244800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:8230800-8245600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:8231000-8250800	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr7:8231000-8252200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:8231200-8245000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr7:8231200-8252400	Weak transcription	Stomach Mucosa	stomach
12	chr7:8231200-8257600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr7:8231400-8275200	Weak transcription	Esophagus	oesophagus
14	chr7:8232600-8246800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:8233200-8244400	Weak transcription	Fetal Stomach	stomach
16	chr7:8238400-8245400	Weak transcription	Right Ventricle	heart
17	chr7:8238400-8253200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:8238600-8249200	Enhancers	Adipose Nuclei	Adipose
19	chr7:8240200-8245600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:8240400-8245400	Weak transcription	Right Atrium	heart
21	chr7:8241600-8245400	Weak transcription	Fetal Intestine Small	intestine
22	chr7:8241800-8245000	Weak transcription	Fetal Heart	heart
23	chr7:8241800-8245200	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr7:8241800-8245400	Weak transcription	Left Ventricle	heart
25	chr7:8241800-8250400	Weak transcription	Gastric	stomach
26	chr7:8241800-8252200	Weak transcription	Pancreas	Pancrea
27	chr7:8241800-8257800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr7:8242000-8253000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:8242000-8253800	Weak transcription	Primary hematopoietic stem cells	blood
30	chr7:8242400-8244400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:8242400-8250400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr7:8242600-8245000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:8242600-8254000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr7:8242800-8245000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:8242800-8253000	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr7:8243400-8254600	Weak transcription	Fetal Intestine Large	intestine
37	chr7:8243600-8251000	Weak transcription	Lung	lung
38	chr7:8244000-8246800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:8244400-8245400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:8244400-8245800	Enhancers	Fetal Stomach	stomach
41	chr7:8244800-8245000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:8244800-8245200	Enhancers	Colon Smooth Muscle	Colon
43	chr7:8244800-8247000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr7:8245000-8245800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:8245000-8246000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:8245000-8246000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:8245000-8246000	Enhancers	Fetal Heart	heart
48	chr7:8245000-8246000	Enhancers	Stomach Smooth Muscle	stomach
49	chr7:8245200-8246400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr7:8245200-8246600	Enhancers	Primary neutrophils fromperipheralblood	blood

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