Variant report

Variant	nsv818650
Chromosome Location	chr8:114574863-115477600
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2472)
CpG islands
(count:367)
Chromatin interactive
region (count:40)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2472 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:114720963-114720970	K562	blood:	n/a	n/a
2	ATF1	chr8:114602201-114602508	K562	blood:	n/a	n/a
3	ATF1	chr8:115228160-115228264	K562	blood:	n/a	n/a
4	ATF1	chr8:114822095-114822305	K562	blood:	n/a	n/a
5	ATF2	chr8:114696927-114697818	GM12878	blood:	n/a	n/a
6	ATF2	chr8:114687470-114687947	GM12878	blood:	n/a	n/a
7	ATF2	chr8:115309934-115311300	GM12878	blood:	n/a	n/a
8	ATF2	chr8:114687413-114687961	GM12878	blood:	n/a	n/a
9	ATF2	chr8:114697164-114697813	GM12878	blood:	n/a	n/a
10	ATF2	chr8:115309455-115309795	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr8:114616410-114616887	GM12878	blood:	n/a	n/a
12	ATF2	chr8:115309885-115311242	GM12878	blood:	n/a	n/a
13	ATF2	chr8:115310219-115310638	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:115027320-115027328	K562	blood:	n/a	n/a
15	BACH1	chr8:115330646-115330834	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:115332200-115332247	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:114890099-114890104	K562	blood:	n/a	n/a
18	BACH1	chr8:115226424-115226479	K562	blood:	n/a	n/a
19	BACH1	chr8:114848077-114848163	K562	blood:	n/a	n/a
20	BACH1	chr8:114936321-114936398	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:115441617-115441711	K562	blood:	n/a	n/a
22	BACH1	chr8:114627036-114627067	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr8:115318701-115318964	GM12878	blood:	n/a	chr8:115318871-115318882
24	BATF	chr8:114687598-114687903	GM12878	blood:	n/a	n/a
25	BATF	chr8:115281695-115281857	GM12878	blood:	n/a	n/a
26	BATF	chr8:114697001-114697705	GM12878	blood:	n/a	n/a
27	BATF	chr8:115310578-115311176	GM12878	blood:	n/a	n/a
28	BATF	chr8:115282793-115283090	GM12878	blood:	n/a	n/a
29	BATF	chr8:115447401-115447735	GM12878	blood:	n/a	n/a
30	BATF	chr8:115451366-115451632	GM12878	blood:	n/a	n/a
31	BATF	chr8:114752604-114752779	GM12878	blood:	n/a	chr8:114752701-114752711 chr8:114752700-114752711 chr8:114752705-114752715
32	BATF	chr8:114697315-114697659	GM12878	blood:	n/a	n/a
33	BATF	chr8:114616421-114616811	GM12878	blood:	n/a	chr8:114616655-114616666
34	BATF	chr8:114616476-114616789	GM12878	blood:	n/a	chr8:114616655-114616666
35	BATF	chr8:115310001-115310427	GM12878	blood:	n/a	n/a
36	BATF	chr8:114628233-114628445	GM12878	blood:	n/a	chr8:114628409-114628418
37	BATF	chr8:115451370-115451612	GM12878	blood:	n/a	n/a
38	BATF	chr8:115309992-115310599	GM12878	blood:	n/a	n/a
39	BATF	chr8:115447376-115447721	GM12878	blood:	n/a	n/a
40	BATF	chr8:115310640-115310938	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:115310015-115310397	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:114697283-114697743	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:114616465-114616808	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:114628223-114628450	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:115310650-115310937	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:115310567-115311162	GM12878	blood:	n/a	n/a
47	BCL11A	chr8:114664594-114664807	GM12878	blood:	n/a	chr8:114664679-114664688
48	BCL11A	chr8:114628249-114628426	GM12878	blood:	n/a	n/a
49	BCL11A	chr8:114697247-114697780	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:114697011-114697230	GM12878	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:115466108-115466158	AG09319	gingival:	n/a
2	chr8:115466108-115466158	AG09319	gingival:	n/a
3	chr8:114896516-114896566	HMEC	breast:	n/a
4	chr8:115020418-115020468	HEEpiC	esophagus:	n/a
5	chr8:115020418-115020468	HEK293	kidney:	embryo
6	chr8:115301887-115301937	HNPCEpiC	eye:	n/a
7	chr8:115466108-115466158	BJ	skin:	n/a
8	chr8:114896516-114896566	SK-N-SH_RA	brain:	n/a
9	chr8:115020418-115020468	AG04450	lung:	fetal
10	chr8:114992667-114992717	NHBE	bronchial:	n/a
11	chr8:114992667-114992717	T-47D	breast:	n/a
12	chr8:115020418-115020468	PrEC	prostate:	n/a
13	chr8:114896516-114896566	AoSMC	blood vessel:	n/a
14	chr8:115466108-115466158	T-47D	breast:	n/a
15	chr8:115301887-115301937	HCM	heart:	n/a
16	chr8:115301887-115301937	NH-A	brain:	n/a
17	chr8:115301887-115301937	RPTEC	kidney:	n/a
18	chr8:114992667-114992717	Caco-2	colon:	n/a
19	chr8:115466108-115466158	K562	blood:	n/a
20	chr8:114992667-114992717	HepG2	liver:	n/a
21	chr8:115301887-115301937	Jurkat	blood:	n/a
22	chr8:115020418-115020468	IMR90	lung:	fetal
23	chr8:115466108-115466158	SAEC	small airway:	n/a
24	chr8:115301887-115301937	IMR90	lung:	fetal
25	chr8:115301887-115301937	MCF-7	breast:	n/a
26	chr8:115020418-115020468	MCF-7	breast:	n/a
27	chr8:115466108-115466158	AG04449	skin:	fetal
28	chr8:115466108-115466158	ProgFib	skin:	n/a
29	chr8:115398676-115398726	SK-N-SH	brain:	n/a
30	chr8:114896516-114896566	HepG2	liver:	n/a
31	chr8:115301887-115301937	HMEC	breast:	n/a
32	chr8:115398676-115398726	NB4	blood:	n/a
33	chr8:114992667-114992717	SAEC	small airway:	n/a
34	chr8:114896516-114896566	AG04450	lung:	fetal
35	chr8:114992667-114992717	HEK293	kidney:	embryo
36	chr8:115020418-115020468	CMK	blood:	n/a
37	chr8:115398676-115398726	NHBE	bronchial:	n/a
38	chr8:115398676-115398726	HRPEpiC	eye:	n/a
39	chr8:115301887-115301937	AoSMC	blood vessel:	n/a
40	chr8:114896516-114896566	PrEC	prostate:	n/a
41	chr8:115398676-115398726	GM12891	blood:	n/a
42	chr8:114992667-114992717	MCF-7	breast:	n/a
43	chr8:114992667-114992717	AG09319	gingival:	n/a
44	chr8:114992667-114992717	HEEpiC	esophagus:	n/a
45	chr8:115020418-115020468	ProgFib	skin:	n/a
46	chr8:114896516-114896566	HEEpiC	esophagus:	n/a
47	chr8:115020418-115020468	NHBE	bronchial:	n/a
48	chr8:115466108-115466158	PANC-1	pancreas:	n/a
49	chr8:115466108-115466158	SK-N-SH_RA	brain:	n/a
50	chr8:114896516-114896566	HCF	heart:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
2	chr17:58590060..58590787-chr8:115060352..115060949,2	MCF-7	breast:
3	chr8:114612946..114615304-chr8:114616262..114619018,2	K562	blood:
4	chr8:114728056..114730786-chr8:114735490..114737141,2	MCF-7	breast:
5	chr3:133848002..133849522-chr8:115073919..115075439,2	K562	blood:
6	chr8:115466661..115467320-chr8:115801108..115801704,2	MCF-7	breast:
7	chr8:114823206..114825087-chr8:114825819..114828055,2	MCF-7	breast:
8	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
9	chr8:114674540..114677133-chr8:114678204..114681093,2	MCF-7	breast:
10	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:
11	chr8:114966861..114968820-chr8:114970401..114973108,2	MCF-7	breast:
12	chr8:114816422..114818283-chr8:114819579..114821682,2	K562	blood:
13	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:
14	chr8:115308430..115310814-chr8:115329605..115331962,2	MCF-7	breast:
15	chr8:115313320..115315368-chr8:115318316..115320811,2	K562	blood:
16	chr8:114966861..114968820-chr8:114970401..114973108,2	MCF-7	breast:
17	chr8:114726767..114728382-chr8:114731029..114732643,2	K562	blood:
18	chr8:114666240..114668992-chr8:114678548..114680585,2	K562	blood:
19	chr8:114728056..114730786-chr8:114735490..114737141,2	MCF-7	breast:
20	chr8:115023596..115026093-chr8:115027615..115029686,2	K562	blood:
21	chr8:115239390..115241790-chr8:115242578..115244996,2	K562	blood:
22	chr8:115239390..115241790-chr8:115242578..115244996,2	K562	blood:
23	chr8:114612946..114615304-chr8:114616262..114619018,2	K562	blood:
24	chr8:114478442..114479179-chr8:115103168..115103714,3	MCF-7	breast:
25	chr8:114384438..114385053-chr8:114992865..114993457,2	MCF-7	breast:
26	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
27	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
28	chr8:114674540..114677133-chr8:114678204..114681093,2	MCF-7	breast:
29	chr8:114854128..114856443-chr8:114857146..114858735,2	MCF-7	breast:
30	chr6:55668603..55669259-chr8:114927462..114928176,2	MCF-7	breast:
31	chr8:114823206..114825087-chr8:114825819..114828055,2	MCF-7	breast:
32	chr8:115327227..115329633-chr8:115330616..115333275,2	MCF-7	breast:
33	chr8:114816422..114818283-chr8:114819579..114821682,2	K562	blood:
34	chr8:114726767..114728382-chr8:114731029..114732643,2	K562	blood:
35	chr8:114666240..114668992-chr8:114678548..114680585,2	K562	blood:
36	chr8:115023596..115026093-chr8:115027615..115029686,2	K562	blood:
37	chr7:150045798..150047502-chr8:114590956..114592459,2	MCF-7	breast:
38	chr8:114854128..114856443-chr8:114857146..114858735,2	MCF-7	breast:
39	chr8:115468981..115471423-chr8:115486430..115487982,2	MCF-7	breast:
40	chr8:115313320..115315368-chr8:115318316..115320811,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD3-6	chr8:115330629-115331140	NONHSAT128358
2	lnc-CSMD3-5	chr8:115308063-115308898	NONHSAT128356
3	lnc-CSMD3-1	chr8:115316636-115316724	XLOC_007184
4	lnc-CSMD3-5	chr8:115309415-115309984	NONHSAT128356
5	lnc-CSMD3-1	chr8:115323322-115323497	XLOC_007184
6	lnc-CSMD3-1	chr8:115315119-115315373	XLOC_007184
7	lnc-CSMD3-5	chr8:115299951-115300072	NONHSAT128356

No data

Variant related genes	Relation type
ENSG00000254339	TF binding region
ENSG00000253207	TF binding region
ENSG00000206719	TF binding region
ENSG00000253499	TF binding region
ENSG00000254339	CpG island
ENSG00000253207	CpG island
ENSG00000206719	CpG island
ENSG00000253499	CpG island
ENSG00000253499	chromatin interactions
ENSG00000270553	chromatin interactions
MAGT1	miRNA target sites
MAFK	miRNA target sites

Extended variants
information (count: 9771 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:9771 , 50 per page) page: 1 2 3 4 5 6 7 ... 196

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553566597	chr8:114599425-114599426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs185834674	chr8:114599440-114599441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4492406	chr8:114599447-114599448	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs540710359	chr8:114599468-114599469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556120092	chr8:114599470-114599471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571013724	chr8:114599492-114599493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189811714	chr8:114599585-114599586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78087051	chr8:114599598-114599599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147344319	chr8:114599615-114599616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575235798	chr8:114599651-114599652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181076068	chr8:114599675-114599676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560680189	chr8:114599681-114599682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112054389	chr8:114599682-114599683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114043422	chr8:114599728-114599729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546029452	chr8:114599745-114599746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56207250	chr8:114599768-114599769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs139469484	chr8:114599909-114599910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28475443	chr8:114599959-114599960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548443070	chr8:114599963-114599964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191999399	chr8:114599968-114599969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113424332	chr8:114599993-114599994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547141159	chr8:114600022-114600023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570359015	chr8:114600037-114600038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142527645	chr8:114600057-114600058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73701622	chr8:114600096-114600097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs569608624	chr8:114600098-114600099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535080481	chr8:114600102-114600103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4384009	chr8:114600110-114600111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575147815	chr8:114600180-114600181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534500853	chr8:114600181-114600182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554405669	chr8:114600188-114600189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369996339	chr8:114600205-114600206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577555085	chr8:114600284-114600285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546263194	chr8:114600310-114600311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562869614	chr8:114600314-114600315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188455724	chr8:114600316-114600317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73701623	chr8:114600367-114600368	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs561749361	chr8:114600368-114600369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527576304	chr8:114600429-114600430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12334661	chr8:114600437-114600438	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs191984489	chr8:114600448-114600449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533005969	chr8:114600469-114600470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549967350	chr8:114600511-114600512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537235067	chr8:114600523-114600524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535549366	chr8:114600656-114600657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548954062	chr8:114600687-114600688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139542435	chr8:114600693-114600694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116961338	chr8:114600694-114600695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7010793	chr8:114600819-114600820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs60837504	chr8:114600847-114600848	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:114599400-114607400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:114605400-114605800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:114613800-114614400	Enhancers	Brain Hippocampus Middle	brain
4	chr8:114613800-114614400	Enhancers	Brain Substantia Nigra	brain
5	chr8:114614000-114614400	Enhancers	Brain Anterior Caudate	brain
6	chr8:114614000-114614400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr8:114614200-114615000	Enhancers	Brain Cingulate Gyrus	brain
8	chr8:114614400-114615400	Weak transcription	Brain Hippocampus Middle	brain
9	chr8:114615600-114615800	Enhancers	Brain Hippocampus Middle	brain
10	chr8:114615600-114616000	Enhancers	Dnd41	blood
11	chr8:114630000-114630400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:114631600-114632000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:114632000-114632400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:114632400-114633600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:114644000-114644200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:114644000-114644200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:114644200-114645200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr8:114644200-114645200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:114644600-114645800	ZNF genes & repeats	Dnd41	blood
20	chr8:114645200-114645600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:114645200-114645600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:114645400-114646000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:114645600-114645800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr8:114645600-114646200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:114645800-114646000	Weak transcription	Dnd41	blood
26	chr8:114645800-114646200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:114646000-114647600	Enhancers	Dnd41	blood
28	chr8:114646200-114646400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:114646200-114646400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr8:114656200-114656600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:114664400-114665600	Enhancers	Primary B cells from cord blood	blood
32	chr8:114668600-114669400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:114668800-114669400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:114671400-114674200	Enhancers	Primary B cells from peripheral blood	blood
35	chr8:114671600-114672600	Enhancers	Primary B cells from cord blood	blood
36	chr8:114672600-114673600	Weak transcription	Primary B cells from cord blood	blood
37	chr8:114673600-114674400	Enhancers	Primary B cells from cord blood	blood
38	chr8:114674200-114676600	Weak transcription	Primary B cells from peripheral blood	blood
39	chr8:114676600-114677200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
40	chr8:114676800-114677200	ZNF genes & repeats	Dnd41	blood
41	chr8:114677200-114677800	Weak transcription	Primary B cells from peripheral blood	blood
42	chr8:114677800-114678200	Enhancers	Primary B cells from peripheral blood	blood
43	chr8:114677800-114678200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr8:114696000-114697800	Active TSS	Brain Anterior Caudate	brain
45	chr8:114696400-114697000	Enhancers	Primary B cells from cord blood	blood
46	chr8:114696400-114697200	Enhancers	GM12878-XiMat	blood
47	chr8:114696800-114698200	Enhancers	Primary B cells from peripheral blood	blood
48	chr8:114697000-114697200	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr8:114697000-114697400	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr8:114697000-114698200	Enhancers	Primary monocytes fromperipheralblood	blood

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