Variant report

Variant	nsv1031658
Chromosome Location	chr7:127266882-127376775
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2180)
CpG islands
(count:1714)
Chromatin interactive
region (count:164)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2180 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:127291273-127292365	K562	blood:	n/a	n/a
2	ARID3A	chr7:127293418-127293528	K562	blood:	n/a	n/a
3	ARID3A	chr7:127295810-127296083	K562	blood:	n/a	n/a
4	ARID3A	chr7:127291685-127293024	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:127292668-127293100	K562	blood:	n/a	n/a
6	ARID3A	chr7:127290523-127290608	K562	blood:	n/a	n/a
7	ATF1	chr7:127291416-127292340	K562	blood:	n/a	chr7:127291969-127291983
8	ATF2	chr7:127291168-127292110	H1-hESC	embryonic stem cell:	n/a	chr7:127291969-127291983
9	ATF2	chr7:127291324-127292509	H1-hESC	embryonic stem cell:	n/a	chr7:127291969-127291983
10	ATF2	chr7:127324105-127324646	GM12878	blood:	n/a	n/a
11	ATF2	chr7:127291518-127292236	GM12878	blood:	n/a	chr7:127291969-127291983
12	ATF2	chr7:127291504-127292442	GM12878	blood:	n/a	chr7:127291969-127291983
13	ATF2	chr7:127318897-127319333	GM12878	blood:	n/a	n/a
14	ATF2	chr7:127318820-127319468	GM12878	blood:	n/a	n/a
15	ATF3	chr7:127291673-127292283	A549	lung:	n/a	n/a
16	ATF3	chr7:127291653-127292280	K562	blood:	n/a	n/a
17	ATF3	chr7:127291643-127292093	K562	blood:	n/a	chr7:127291645-127291654
18	BACH1	chr7:127291689-127292077	K562	blood:	n/a	n/a
19	BACH1	chr7:127368684-127368693	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:127292436-127292476	K562	blood:	n/a	n/a
21	BACH1	chr7:127293125-127293248	K562	blood:	n/a	n/a
22	BACH1	chr7:127291386-127292396	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr7:127324206-127324538	GM12878	blood:	n/a	n/a
24	BATF	chr7:127319158-127319384	GM12878	blood:	n/a	n/a
25	BATF	chr7:127307086-127307365	GM12878	blood:	n/a	n/a
26	BATF	chr7:127291756-127292134	GM12878	blood:	n/a	n/a
27	BATF	chr7:127319071-127319403	GM12878	blood:	n/a	n/a
28	BCL3	chr7:127324155-127324588	GM12878	blood:	n/a	chr7:127324250-127324257 chr7:127324557-127324566
29	BCL3	chr7:127292008-127292927	A549	lung:	n/a	chr7:127292229-127292238 chr7:127292153-127292166
30	BCL3	chr7:127307071-127307466	GM12878	blood:	n/a	n/a
31	BCLAF1	chr7:127291043-127292580	GM12878	blood:	n/a	chr7:127291646-127291659 chr7:127292229-127292238 chr7:127292153-127292166 chr7:127291650-127291663
32	BCLAF1	chr7:127318887-127319417	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:127291270-127293277	K562	blood:	n/a	n/a
34	BHLHE40	chr7:127275855-127275880	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:127318884-127319276	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:127294447-127294798	K562	blood:	n/a	n/a
37	BHLHE40	chr7:127269470-127269525	K562	blood:	n/a	n/a
38	BHLHE40	chr7:127348825-127349044	K562	blood:	n/a	n/a
39	BHLHE40	chr7:127291090-127292453	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:127295920-127296120	K562	blood:	n/a	n/a
41	BHLHE40	chr7:127291593-127292656	HepG2	liver:	n/a	n/a
42	BHLHE40	chr7:127290541-127290589	K562	blood:	n/a	n/a
43	BRCA1	chr7:127291657-127292307	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr7:127291446-127291983	HepG2	liver:	n/a	n/a
45	BRCA1	chr7:127292223-127292373	HepG2	liver:	n/a	n/a
46	BRCA1	chr7:127292023-127292128	H1-hESC	embryonic stem cell:	n/a	n/a
47	CBX3	chr7:127291013-127293334	K562	blood:	n/a	n/a
48	CBX3	chr7:127291140-127292456	K562	blood:	n/a	n/a
49	CBX3	chr7:127348760-127349375	K562	blood:	n/a	chr7:127348823-127348834
50	CCNT2	chr7:127312914-127313015	K562	blood:	n/a	n/a

(count:1714 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127292389-127292439	ECC-1	luminal epithelium:	n/a
2	chr7:127344973-127345023	HNPCEpiC	eye:	n/a
3	chr7:127292125-127292175	MCF-7	breast:	n/a
4	chr7:127295153-127295203	LNCaP	prostate:	n/a
5	chr7:127314628-127314678	GM19239	blood:	n/a
6	chr7:127292550-127292600	HMEC	breast:	n/a
7	chr7:127292389-127292439	ECC-1	luminal epithelium:	n/a
8	chr7:127344973-127345023	HNPCEpiC	eye:	n/a
9	chr7:127292125-127292175	MCF-7	breast:	n/a
10	chr7:127295153-127295203	LNCaP	prostate:	n/a
11	chr7:127314628-127314678	GM19239	blood:	n/a
12	chr7:127292550-127292600	HMEC	breast:	n/a
13	chr7:127291747-127291797	Caco-2	colon:	n/a
14	chr7:127292223-127292273	T-47D	breast:	n/a
15	chr7:127307809-127307859	PrEC	prostate:	n/a
16	chr7:127292125-127292175	HAEpiC	amniotic membrane:	n/a
17	chr7:127292223-127292273	AoSMC	blood vessel:	n/a
18	chr7:127291747-127291797	HRCEpiC	kidney:	n/a
19	chr7:127269283-127269333	HUVEC	blood vessel:	n/a
20	chr7:127292550-127292600	HUVEC	blood vessel:	n/a
21	chr7:127283926-127283976	MCF10A-Er-Src	breast:	n/a
22	chr7:127365616-127365666	RPTEC	kidney:	n/a
23	chr7:127314628-127314678	PANC-1	pancreas:	n/a
24	chr7:127292158-127292208	HRCEpiC	kidney:	n/a
25	chr7:127307809-127307859	HIPEpiC	eye:	n/a
26	chr7:127269283-127269333	NH-A	brain:	n/a
27	chr7:127340829-127340879	SK-N-SH	brain:	n/a
28	chr7:127288996-127289046	GM12878	blood:	n/a
29	chr7:127292389-127292439	HCT-116	colon:	n/a
30	chr7:127292117-127292167	K562	blood:	n/a
31	chr7:127365616-127365666	SKMC	muscle:	n/a
32	chr7:127292180-127292230	K562	blood:	n/a
33	chr7:127288996-127289046	NT2-D1	testis:	n/a
34	chr7:127314628-127314678	HAEpiC	amniotic membrane:	n/a
35	chr7:127292389-127292439	HL-60	blood:	n/a
36	chr7:127291444-127291494	H1-hESC	embryonic stem cell:	embryo
37	chr7:127314628-127314678	NHDF-neo	bronchial:	n/a
38	chr7:127291444-127291494	HIPEpiC	eye:	n/a
39	chr7:127292158-127292208	RPTEC	kidney:	n/a
40	chr7:127288996-127289046	BJ	skin:	n/a
41	chr7:127307809-127307859	CMK	blood:	n/a
42	chr7:127340829-127340879	SK-N-SH_RA	brain:	n/a
43	chr7:127292223-127292273	Jurkat	blood:	n/a
44	chr7:127269283-127269333	NB4	blood:	n/a
45	chr7:127292223-127292273	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:127318550-127318600	SK-N-SH_RA	brain:	n/a
47	chr7:127371565-127371615	HepG2	liver:	n/a
48	chr7:127329180-127329230	HAEpiC	amniotic membrane:	n/a
49	chr7:127307809-127307859	HAEpiC	amniotic membrane:	n/a
50	chr7:127292117-127292167	LNCaP	prostate:	n/a

(count:164 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:127354365..127356905-chr7:127361625..127363196,2	K562	blood:
2	chr7:127332465..127334198-chr7:127341360..127343562,2	MCF-7	breast:
3	chr7:127267628..127269404-chr7:127274222..127276014,2	K562	blood:
4	chr20:9983318..9983838-chr7:127291405..127291953,2	Hela-S3	cervix:
5	chr7:127354964..127357092-chr7:127358682..127360434,2	K562	blood:
6	chr7:127292301..127294616-chr7:127313829..127315529,2	MCF-7	breast:
7	chr7:127273906..127277056-chr7:127286776..127289218,4	K562	blood:
8	chr7:127226904..127229652-chr7:127273022..127275152,3	K562	blood:
9	chr7:127349984..127350918-chr7:127849791..127850455,2	MCF-7	breast:
10	chr7:127298406..127301093-chr7:127304305..127307205,3	MCF-7	breast:
11	chr7:127371965..127374566-chr7:127386908..127389134,2	K562	blood:
12	chr7:127342487..127344378-chr7:127375148..127377215,2	K562	blood:
13	chr7:127291582..127293542-chr7:127297327..127299302,5	MCF-7	breast:
14	chr7:127226810..127231119-chr7:127290066..127293801,4	MCF-7	breast:
15	chr1:16840307..16840955-chr7:127291583..127292147,2	Hela-S3	cervix:
16	chr7:127292301..127294616-chr7:127313829..127315529,2	MCF-7	breast:
17	chr7:127322349..127324124-chr7:127326869..127328716,2	MCF-7	breast:
18	chr7:127282540..127285250-chr7:127290240..127292394,2	MCF-7	breast:
19	chr7:127321239..127323993-chr7:127348040..127350478,2	K562	blood:
20	chr7:127293455..127295442-chr7:127314786..127317703,2	K562	blood:
21	chr7:127275495..127277111-chr7:127290605..127292857,2	MCF-7	breast:
22	chr7:127274788..127276346-chr7:127281698..127283951,2	MCF-7	breast:
23	chr7:127292643..127294147-chr7:127310003..127312142,2	MCF-7	breast:
24	chr7:127223375..127232960-chr7:127286940..127295803,24	K562	blood:
25	chr7:127226125..127229974-chr7:127289784..127293571,8	MCF-7	breast:
26	chr7:127348829..127352435-chr7:127355750..127359950,4	K562	blood:
27	chr7:127268675..127271053-chr7:127289533..127291398,3	MCF-7	breast:
28	chr7:127364711..127367506-chr7:127369720..127371248,2	MCF-7	breast:
29	chr7:127342221..127343949-chr7:127655072..127657192,2	K562	blood:
30	chr7:127342487..127344378-chr7:127375148..127377215,2	K562	blood:
31	chr7:127363157..127364758-chr7:127370490..127372919,2	K562	blood:
32	chr7:127313118..127315659-chr7:127324018..127326233,2	MCF-7	breast:
33	chr7:127267628..127269404-chr7:127274222..127276014,2	K562	blood:
34	chr7:127289933..127293369-chr7:127304978..127309849,8	MCF-7	breast:
35	chr7:127363018..127366026-chr7:127367125..127369861,3	K562	blood:
36	chr1:212781981..212782558-chr7:127291551..127292258,2	Hela-S3	cervix:
37	chr7:127348587..127349380-chr7:127650287..127651017,2	MCF-7	breast:
38	chr7:127268675..127271053-chr7:127289533..127291398,3	MCF-7	breast:
39	chr7:127289745..127292674-chr7:127316205..127318087,2	K562	blood:
40	chr7:127324074..127325812-chr7:127338072..127340357,2	K562	blood:
41	chr13:46038900..46039511-chr7:127291480..127292315,2	Hela-S3	cervix:
42	chr7:127238051..127238964-chr7:127269066..127269762,2	MCF-7	breast:
43	chr7:127222868..127230871-chr7:127290370..127294912,16	K562	blood:
44	chr7:127304778..127307957-chr7:127308207..127312906,6	K562	blood:
45	chr7:127347508..127350388-chr7:127360932..127362675,2	K562	blood:
46	chr7:127292635..127294692-chr7:127327406..127330053,2	MCF-7	breast:
47	chr7:127224289..127226040-chr7:127290840..127293019,2	MCF-7	breast:
48	chr7:127339061..127341983-chr7:127343851..127345821,2	MCF-7	breast:
49	chr7:127350301..127352881-chr7:127354512..127357487,2	MCF-7	breast:
50	chr2:54683448..54684022-chr7:127291404..127292021,2	HCT-116	colon:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAX4-1	chr7:127284739-127284781	XLOC_006596
2	lnc-PAX4-1	chr7:127291727-127292066	XLOC_006596
3	lnc-PAX4-1	chr7:127285110-127285221	XLOC_006596
4	lnc-PAX4-1	chr7:127284471-127284781	XLOC_006596
5	lnc-PAX4-1	chr7:127285110-127285304	XLOC_006596

No data

Variant related genes	Relation type
SND1	TF binding region
ENSG00000240790	TF binding region
SND1	CpG island
ENSG00000240790	CpG island
ENSG00000048405	chromatin interactions
ENSG00000004059	chromatin interactions
ENSG00000085231	chromatin interactions
ENSG00000207705	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000010292	chromatin interactions
ENSG00000144827	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000196116	chromatin interactions
ENSG00000257341	chromatin interactions
ENSG00000240790	chromatin interactions
ENSG00000162772	chromatin interactions
ENSG00000106328	chromatin interactions
ENSG00000152942	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000106331	chromatin interactions
ENSG00000111639	chromatin interactions
ENSG00000136152	chromatin interactions
ENSG00000197157	chromatin interactions
ENSG00000179562	chromatin interactions
ENSG00000213145	chromatin interactions

Extended variants
information (count: 3637 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3637 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs806190	chr7:127266882-127266883	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574923419	chr7:127266930-127266931	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs189515140	chr7:127266956-127266957	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs146919187	chr7:127267025-127267026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374099345	chr7:127267026-127267027	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs551762656	chr7:127267075-127267076	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs182301321	chr7:127267141-127267142	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186919769	chr7:127267169-127267170	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs562319646	chr7:127267182-127267183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs191940554	chr7:127267191-127267192	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551280507	chr7:127267200-127267201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs569250596	chr7:127267217-127267218	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs539873200	chr7:127267219-127267220	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150666659	chr7:127267303-127267304	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs7799837	chr7:127267314-127267315	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs139539353	chr7:127267315-127267316	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs112061755	chr7:127267412-127267413	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs181565138	chr7:127267413-127267414	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs149692943	chr7:127267468-127267469	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535357849	chr7:127267489-127267490	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs375613598	chr7:127267516-127267517	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574884907	chr7:127267579-127267580	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545440351	chr7:127267600-127267601	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs145497053	chr7:127267601-127267602	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368889572	chr7:127267628-127267629	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543940468	chr7:127267684-127267685	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs139107213	chr7:127267728-127267729	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs185713354	chr7:127267758-127267759	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs75614257	chr7:127267784-127267785	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs190080727	chr7:127267813-127267814	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs57140865	chr7:127267866-127267867	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs35886676	chr7:127267875-127267876	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs563213465	chr7:127267877-127267878	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533358899	chr7:127267920-127267921	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs139963445	chr7:127267960-127267961	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs551750978	chr7:127267975-127267976	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs552963353	chr7:127267988-127267989	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577750188	chr7:127267993-127267994	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs566881372	chr7:127267996-127267997	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs200255108	chr7:127267997-127267998	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs527749833	chr7:127268015-127268016	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs371500104	chr7:127268022-127268023	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs182443263	chr7:127268025-127268026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs576135255	chr7:127268039-127268040	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs201460107	chr7:127268040-127268041	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs141696325	chr7:127268042-127268043	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375151163	chr7:127268043-127268044	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs568148060	chr7:127268063-127268064	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs567746649	chr7:127268078-127268079	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs142434527	chr7:127268096-127268097	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Glioblastoma multiforme	21510904	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Myxofibrosarcoma	20639860	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:3919 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127261000-127269600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:127261400-127267200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:127267200-127267400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:127267400-127268200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:127268200-127269800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:127268600-127268800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:127268600-127268800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr7:127268600-127269000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr7:127268800-127269400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr7:127268800-127269600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:127268800-127269600	Enhancers	Duodenum Mucosa	Duodenum
12	chr7:127268800-127269800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:127268800-127269800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr7:127268800-127269800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:127268800-127269800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:127268800-127269800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:127268800-127269800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:127268800-127272200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr7:127268800-127272200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:127269000-127269200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr7:127269000-127269600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr7:127269000-127269800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:127269000-127269800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr7:127269000-127269800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:127269200-127269600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:127269400-127269600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:127269400-127269800	Enhancers	Primary B cells from peripheral blood	blood
28	chr7:127269400-127269800	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr7:127269400-127269800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr7:127269400-127269800	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr7:127269400-127269800	Enhancers	Placenta	Placenta
32	chr7:127269400-127269800	Enhancers	Spleen	Spleen
33	chr7:127269600-127269800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr7:127269600-127269800	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr7:127269600-127269800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:127269600-127269800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:127269600-127269800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
38	chr7:127269600-127269800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr7:127269600-127269800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr7:127269600-127269800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:127269600-127269800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
42	chr7:127269600-127269800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:127269600-127269800	Flanking Active TSS	Duodenum Mucosa	Duodenum
44	chr7:127269600-127269800	Enhancers	Placenta Amnion	Placenta Amnion
45	chr7:127269600-127269800	Enhancers	HepG2	liver
46	chr7:127269600-127269800	Enhancers	Osteobl	bone
47	chr7:127269600-127270000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:127269800-127270000	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr7:127269800-127270000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:127269800-127271200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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