Variant report

Variant	nsv887433
Chromosome Location	chr7:6557135-6668027
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3586)
CpG islands
(count:4458)
Chromatin interactive
region (count:142)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3586 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6629468-6629712	K562	blood:	n/a	n/a
2	ARID3A	chr7:6629531-6629849	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:6614192-6614418	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:6615037-6615691	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:6605349-6605650	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:6614150-6614475	K562	blood:	n/a	n/a
7	ARID3A	chr7:6616934-6617136	K562	blood:	n/a	n/a
8	ARID3A	chr7:6598567-6598706	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:6616649-6617363	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:6583036-6583373	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:6618274-6618393	K562	blood:	n/a	n/a
12	ARID3A	chr7:6618130-6618589	HepG2	liver:	n/a	n/a
13	ATF1	chr7:6652571-6652812	K562	blood:	n/a	n/a
14	ATF1	chr7:6616890-6617293	K562	blood:	n/a	n/a
15	ATF1	chr7:6618390-6618532	K562	blood:	n/a	n/a
16	ATF2	chr7:6616962-6617218	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr7:6629394-6629712	GM12878	blood:	n/a	n/a
18	ATF2	chr7:6616892-6617306	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr7:6616855-6617276	GM12878	blood:	n/a	n/a
20	ATF2	chr7:6593208-6593692	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr7:6593225-6593689	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr7:6616856-6617355	GM12878	blood:	n/a	n/a
23	ATF3	chr7:6616841-6617244	K562	blood:	n/a	n/a
24	ATF3	chr7:6616918-6617188	K562	blood:	n/a	n/a
25	ATF3	chr7:6629337-6629771	A549	lung:	n/a	chr7:6629523-6629532 chr7:6629564-6629584
26	ATF3	chr7:6629344-6630003	A549	lung:	n/a	chr7:6629523-6629532 chr7:6629564-6629584
27	BACH1	chr7:6566096-6566354	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:6570414-6570938	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr7:6629362-6630071	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr7:6617014-6617175	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr7:6630335-6630344	K562	blood:	n/a	n/a
32	BACH1	chr7:6586728-6586798	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr7:6659295-6659530	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:6616917-6617253	GM12878	blood:	n/a	chr7:6617026-6617035
35	BCL3	chr7:6662021-6662558	GM12878	blood:	n/a	chr7:6662039-6662052 chr7:6662045-6662058 chr7:6662050-6662059 chr7:6662047-6662056 chr7:6662040-6662053 chr7:6662044-6662053 chr7:6662036-6662049
36	BCL3	chr7:6611092-6611440	GM12878	blood:	n/a	n/a
37	BCL3	chr7:6616889-6617225	GM12878	blood:	n/a	chr7:6617026-6617035
38	BCL3	chr7:6611031-6611500	GM12878	blood:	n/a	n/a
39	BCL3	chr7:6662073-6662402	GM12878	blood:	n/a	n/a
40	BCL3	chr7:6629789-6630335	A549	lung:	n/a	chr7:6629794-6629807 chr7:6629869-6629878 chr7:6629872-6629881 chr7:6629799-6629812
41	BCL3	chr7:6629362-6630010	GM12878	blood:	n/a	chr7:6629794-6629807 chr7:6629869-6629878 chr7:6629872-6629881 chr7:6629775-6629788 chr7:6629561-6629574 chr7:6629733-6629746 chr7:6629799-6629812
42	BCLAF1	chr7:6641859-6642232	GM12878	blood:	n/a	n/a
43	BCLAF1	chr7:6616883-6617349	GM12878	blood:	n/a	chr7:6617026-6617035
44	BCLAF1	chr7:6629326-6630156	GM12878	blood:	n/a	chr7:6629794-6629807 chr7:6629869-6629878 chr7:6629872-6629881 chr7:6629775-6629788 chr7:6629561-6629574 chr7:6629733-6629746 chr7:6629799-6629812
45	BCLAF1	chr7:6616882-6617340	GM12878	blood:	n/a	chr7:6617026-6617035
46	BCLAF1	chr7:6629293-6630019	GM12878	blood:	n/a	chr7:6629794-6629807 chr7:6629869-6629878 chr7:6629872-6629881 chr7:6629775-6629788 chr7:6629561-6629574 chr7:6629733-6629746 chr7:6629799-6629812
47	BHLHE40	chr7:6585459-6585787	GM12878	blood:	n/a	chr7:6585463-6585479
48	BHLHE40	chr7:6559927-6560142	K562	blood:	n/a	n/a
49	BHLHE40	chr7:6566232-6566261	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:6616905-6617316	GM12878	blood:	n/a	n/a

(count:4458 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6644352-6644402	Hela-S3	cervix:	n/a
2	chr7:6616919-6616969	MCF10A-Er-Src	breast:	n/a
3	chr7:6592322-6592372	AG04449	skin:	fetal
4	chr7:6655727-6655777	GM12891	blood:	n/a
5	chr7:6617276-6617326	HCM	heart:	n/a
6	chr7:6644352-6644402	Hela-S3	cervix:	n/a
7	chr7:6616919-6616969	MCF10A-Er-Src	breast:	n/a
8	chr7:6592322-6592372	AG04449	skin:	fetal
9	chr7:6655727-6655777	GM12891	blood:	n/a
10	chr7:6617276-6617326	HCM	heart:	n/a
11	chr7:6647955-6648005	HRCEpiC	kidney:	n/a
12	chr7:6661804-6661854	Jurkat	blood:	n/a
13	chr7:6575581-6575631	HRPEpiC	eye:	n/a
14	chr7:6570566-6570616	MCF-7	breast:	n/a
15	chr7:6644352-6644402	HRE	kidney:	n/a
16	chr7:6592322-6592372	HEEpiC	esophagus:	n/a
17	chr7:6659785-6659835	HAEpiC	amniotic membrane:	n/a
18	chr7:6590947-6590997	AG09309	skin:	n/a
19	chr7:6666368-6666418	HIPEpiC	eye:	n/a
20	chr7:6586786-6586836	PANC-1	pancreas:	n/a
21	chr7:6616919-6616969	BJ	skin:	n/a
22	chr7:6648166-6648216	A549	lung:	n/a
23	chr7:6655973-6656023	PrEC	prostate:	n/a
24	chr7:6591968-6592018	MCF-7	breast:	n/a
25	chr7:6576152-6576202	HRPEpiC	eye:	n/a
26	chr7:6659785-6659835	A549	lung:	n/a
27	chr7:6654880-6654930	MCF10A-Er-Src	breast:	n/a
28	chr7:6566649-6566699	AG09309	skin:	n/a
29	chr7:6568476-6568526	RPTEC	kidney:	n/a
30	chr7:6617276-6617326	H1-hESC	embryonic stem cell:	embryo
31	chr7:6590564-6590614	IMR90	lung:	fetal
32	chr7:6655973-6656023	HRE	kidney:	n/a
33	chr7:6651748-6651798	HIPEpiC	eye:	n/a
34	chr7:6576353-6576403	IMR90	lung:	fetal
35	chr7:6568476-6568526	HRCEpiC	kidney:	n/a
36	chr7:6655711-6655761	GM12878	blood:	n/a
37	chr7:6626877-6626927	Hepatocyte	liver:	n/a
38	chr7:6629350-6629400	HMEC	breast:	n/a
39	chr7:6629959-6630009	AG04449	skin:	fetal
40	chr7:6614945-6614995	SAEC	small airway:	n/a
41	chr7:6575968-6576018	HepG2	liver:	n/a
42	chr7:6629806-6629856	ovcar-3	ovarian:	n/a
43	chr7:6566324-6566374	HRPEpiC	eye:	n/a
44	chr7:6630190-6630240	ovcar-3	ovarian:	n/a
45	chr7:6566324-6566374	A549	lung:	n/a
46	chr7:6590564-6590614	SK-N-MC	brain:	n/a
47	chr7:6647402-6647452	HepG2	liver:	n/a
48	chr7:6629002-6629052	AG04449	skin:	fetal
49	chr7:6590564-6590614	SAEC	small airway:	n/a
50	chr7:6565891-6565941	HCF	heart:	n/a

(count:142 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:6645170..6647656-chr7:6721647..6723270,2	K562	blood:
2	chr7:6652722..6654943-chr7:6655850..6658545,2	K562	blood:
3	chr7:6551198..6555280-chr7:6561370..6563899,3	K562	blood:
4	chr7:6628057..6630995-chr7:6646189..6648379,2	K562	blood:
5	chr7:6656839..6659879-chr7:6661538..6663786,3	K562	blood:
6	chr7:6564171..6565673-chr7:6642376..6644316,2	K562	blood:
7	chr7:6628464..6631299-chr7:6640310..6642319,3	K562	blood:
8	chr7:6615703..6619364-chr7:6676501..6679314,4	K562	blood:
9	chr7:6641830..6642345-chr7:6698974..6699620,2	MCF-7	breast:
10	chr7:6615687..6618664-chr7:6627812..6632591,8	MCF-7	breast:
11	chr7:6629361..6631109-chr7:6633004..6635792,5	MCF-7	breast:
12	chr7:6599534..6602029-chr7:6628855..6631430,2	K562	blood:
13	chr7:6666282..6668533-chr7:6675191..6678454,4	MCF-7	breast:
14	chr7:6614289..6616112-chr7:6628784..6631190,2	K562	blood:
15	chr15:59279868..59280764-chr7:6616794..6617468,2	Hela-S3	cervix:
16	chr7:6617184..6619983-chr7:6640766..6643695,2	MCF-7	breast:
17	chr22:37594666..37595464-chr7:6616789..6617450,2	Hela-S3	cervix:
18	chr7:6604596..6607112-chr7:6612334..6613997,2	K562	blood:
19	chr7:6655297..6658106-chr7:6659491..6662615,3	K562	blood:
20	chr7:6660564..6662217-chr7:6683757..6686361,2	MCF-7	breast:
21	chr7:6642714..6644762-chr7:6645777..6647383,2	K562	blood:
22	chr7:6632706..6634553-chr7:6675850..6677818,2	K562	blood:
23	chr7:6632840..6635452-chr7:6636875..6640304,4	K562	blood:
24	chr7:6630383..6633367-chr7:6634117..6636987,2	K562	blood:
25	chr7:6614342..6622557-chr7:6625132..6631922,18	K562	blood:
26	chr7:6612729..6615949-chr7:6673669..6677097,3	K562	blood:
27	chr7:6660007..6662837-chr7:6675219..6677958,3	K562	blood:
28	chr17:49337778..49338372-chr7:6616477..6617139,2	HCT-116	colon:
29	chr7:6582625..6584643-chr7:6586210..6588627,2	K562	blood:
30	chr7:6652934..6655791-chr7:6675915..6678392,2	MCF-7	breast:
31	chr7:6604596..6607112-chr7:6612334..6613997,2	K562	blood:
32	chr7:6615687..6618664-chr7:6627812..6632591,8	MCF-7	breast:
33	chr7:6599967..6601686-chr7:6615495..6617237,2	K562	blood:
34	chr7:6614342..6622557-chr7:6625132..6631922,18	K562	blood:
35	chr7:6628303..6631132-chr7:6637511..6639950,2	K562	blood:
36	chr7:6641239..6643457-chr7:6645179..6647378,2	MCF-7	breast:
37	chr7:6644575..6647418-chr7:6652621..6655088,2	K562	blood:
38	chr7:6036554..6037500-chr7:6641616..6642526,2	K562	blood:
39	chr7:6611446..6613807-chr7:6615572..6617760,2	MCF-7	breast:
40	chr7:6659549..6661363-chr7:6670073..6672008,2	K562	blood:
41	chr7:6628238..6630542-chr7:6653702..6656593,2	MCF-7	breast:
42	chr7:6541570..6543326-chr7:6585489..6588258,2	MCF-7	breast:
43	chr7:6570876..6573831-chr7:6581104..6583743,3	MCF-7	breast:
44	chr7:6627960..6631587-chr7:6636185..6643600,9	MCF-7	breast:
45	chr7:6588615..6590348-chr7:6593540..6596272,2	K562	blood:
46	chr7:6659409..6665689-chr7:6670317..6679304,11	MCF-7	breast:
47	chr7:6630176..6632392-chr7:6634480..6637119,2	K562	blood:
48	chr7:6656839..6659879-chr7:6661538..6663786,3	K562	blood:
49	chr7:6521171..6524635-chr7:6615181..6617344,3	K562	blood:
50	chr7:6617184..6619983-chr7:6640766..6643695,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf26-1	chr7:6621773-6622342	NONHSAT119009
2	lnc-GRID2IP-2	chr7:6616573-6616698	NONHSAT119002
3	lnc-GRID2IP-2	chr7:6616302-6616419	NONHSAT119002
4	lnc-C7orf26-1	chr7:6627278-6627705	NONHSAT119009
5	lnc-C7orf26-1	chr7:6623346-6623463	NONHSAT119009
6	lnc-GRID2IP-1	chr7:6618196-6618272	ENSG00000232581.1
7	lnc-GRID2IP-1	chr7:6628988-6629569	NONHSAT119018
8	lnc-GRID2IP-1	chr7:6628326-6628605	ENSG00000232581.1
9	lnc-GRID2IP-1	chr7:6627741-6628856	NONHSAT119018

No data

Variant related genes	Relation type
GRID2IP	TF binding region
C7orf26	TF binding region
ZNF853	TF binding region
ZDHHC4	TF binding region
ENSG00000232581	TF binding region
GRID2IP	CpG island
C7orf26	CpG island
ZNF853	CpG island
ZDHHC4	CpG island
ENSG00000232581	CpG island
ENSG00000164535	chromatin interactions
ENSG00000120662	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000236609	chromatin interactions
ENSG00000239039	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000110080	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000129696	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000011260	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000133466	chromatin interactions
ENSG00000214194	chromatin interactions
ENSG00000242110	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000215045	chromatin interactions
ENSG00000074603	chromatin interactions
ENSG00000157450	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000265692	chromatin interactions

Extended variants
information (count: 5118 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5118 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10447683	chr7:6557135-6557136	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571678330	chr7:6557146-6557147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532515836	chr7:6557244-6557245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76707454	chr7:6557262-6557263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115434779	chr7:6557263-6557264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142203402	chr7:6557283-6557284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373327974	chr7:6557348-6557349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376407942	chr7:6557354-6557355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369981165	chr7:6557418-6557419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555260103	chr7:6557432-6557433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546584381	chr7:6557453-6557454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146301775	chr7:6557457-6557458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567267171	chr7:6557458-6557459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367545785	chr7:6557478-6557479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534605024	chr7:6557492-6557493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201670978	chr7:6557535-6557536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537533349	chr7:6557552-6557553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139562287	chr7:6557553-6557554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563490092	chr7:6557562-6557563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs58161513	chr7:6557604-6557605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116702010	chr7:6557642-6557643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs74895231	chr7:6557710-6557711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs62441274	chr7:6557712-6557713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372779439	chr7:6557729-6557730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538237031	chr7:6557764-6557765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs117080765	chr7:6557815-6557816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192338837	chr7:6557954-6557955	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575242520	chr7:6558057-6558058	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184714087	chr7:6558091-6558092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569357396	chr7:6558097-6558098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561469542	chr7:6558104-6558105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs373628772	chr7:6558106-6558107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540945019	chr7:6558109-6558110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs558508188	chr7:6558147-6558148	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs565548339	chr7:6558151-6558152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532578370	chr7:6558198-6558199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550683672	chr7:6558228-6558229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563039621	chr7:6558233-6558234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs28504332	chr7:6558262-6558263	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs144301865	chr7:6558279-6558280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558969728	chr7:6558321-6558322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs148736834	chr7:6558324-6558325	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs534474274	chr7:6558336-6558337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs12532604	chr7:6558384-6558385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573154753	chr7:6558474-6558475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs77798396	chr7:6558520-6558521	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534131161	chr7:6558528-6558529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571194418	chr7:6558534-6558535	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs11478136	chr7:6558541-6558542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs398003546	chr7:6558549-6558550	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3713 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6556400-6566000	Weak transcription	Right Atrium	heart
2	chr7:6556600-6559600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr7:6556600-6559600	Weak transcription	Fetal Thymus	thymus
4	chr7:6556600-6559800	Weak transcription	Primary B cells from cord blood	blood
5	chr7:6556600-6560200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:6559600-6560400	Enhancers	Fetal Thymus	thymus
7	chr7:6559600-6560600	Enhancers	Primary B cells from peripheral blood	blood
8	chr7:6559800-6560600	Enhancers	Primary B cells from cord blood	blood
9	chr7:6560000-6560200	Bivalent Enhancer	Placenta	Placenta
10	chr7:6560000-6560600	Bivalent Enhancer	HepG2	liver
11	chr7:6560200-6560400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:6560200-6560400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:6560200-6560400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr7:6560400-6561000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:6560600-6565400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr7:6560600-6565800	Weak transcription	Primary B cells from cord blood	blood
17	chr7:6561000-6561200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:6561000-6561200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:6561000-6561400	Active TSS	Spleen	Spleen
20	chr7:6561200-6565400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:6563200-6563400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:6563400-6564000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:6564000-6564800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:6565200-6566400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:6565400-6565600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:6565400-6566000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:6565400-6566400	Bivalent Enhancer	Fetal Thymus	thymus
28	chr7:6565600-6565800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:6565600-6565800	Enhancers	Primary B cells from peripheral blood	blood
30	chr7:6565600-6565800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr7:6565600-6565800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr7:6565600-6565800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:6565600-6565800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
34	chr7:6565600-6566000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
35	chr7:6565600-6566000	Bivalent Enhancer	Fetal Stomach	stomach
36	chr7:6565600-6566000	Flanking Bivalent TSS/Enh	HepG2	liver
37	chr7:6565600-6566400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:6565600-6566400	Bivalent Enhancer	Fetal Intestine Small	intestine
39	chr7:6565800-6566000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:6565800-6566000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:6565800-6566000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr7:6565800-6566000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
43	chr7:6565800-6566000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:6565800-6566000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr7:6565800-6566000	Bivalent Enhancer	Brain Germinal Matrix	brain
46	chr7:6565800-6566000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr7:6565800-6566000	Bivalent Enhancer	Fetal Brain Female	brain
48	chr7:6565800-6566000	Enhancers	A549	lung
49	chr7:6565800-6566000	Bivalent Enhancer	HMEC	breast
50	chr7:6565800-6566200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood

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