Variant report

Variant	nsv891353
Chromosome Location	chr8:115247555-115526520
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:885)
CpG islands
(count:366)
Chromatin interactive
region (count:19)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:885 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:115309885-115311242	GM12878	blood:	n/a	n/a
2	ATF2	chr8:115310219-115310638	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:115309455-115309795	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:115309934-115311300	GM12878	blood:	n/a	n/a
5	ATF2	chr8:115524683-115525086	GM12878	blood:	n/a	n/a
6	ATF2	chr8:115524667-115525053	GM12878	blood:	n/a	n/a
7	BACH1	chr8:115441617-115441711	K562	blood:	n/a	n/a
8	BACH1	chr8:115330646-115330834	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:115332200-115332247	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr8:115451366-115451632	GM12878	blood:	n/a	n/a
11	BATF	chr8:115281695-115281857	GM12878	blood:	n/a	n/a
12	BATF	chr8:115310001-115310427	GM12878	blood:	n/a	n/a
13	BATF	chr8:115524605-115525084	GM12878	blood:	n/a	chr8:115524859-115524870
14	BATF	chr8:115309992-115310599	GM12878	blood:	n/a	n/a
15	BATF	chr8:115282793-115283090	GM12878	blood:	n/a	n/a
16	BATF	chr8:115447376-115447721	GM12878	blood:	n/a	n/a
17	BATF	chr8:115318701-115318964	GM12878	blood:	n/a	chr8:115318871-115318882
18	BATF	chr8:115447401-115447735	GM12878	blood:	n/a	n/a
19	BATF	chr8:115451370-115451612	GM12878	blood:	n/a	n/a
20	BATF	chr8:115310578-115311176	GM12878	blood:	n/a	n/a
21	BATF	chr8:115310640-115310938	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:115310015-115310397	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:115310650-115310937	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:115310567-115311162	GM12878	blood:	n/a	n/a
25	BCL3	chr8:115310042-115310348	GM12878	blood:	n/a	n/a
26	BCL3	chr8:115310631-115311217	GM12878	blood:	n/a	n/a
27	BCLAF1	chr8:115310652-115311196	GM12878	blood:	n/a	n/a
28	BCLAF1	chr8:115310053-115311206	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:115282801-115283059	GM12878	blood:	n/a	n/a
30	BHLHE40	chr8:115310002-115311236	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:115281742-115281877	GM12878	blood:	n/a	n/a
32	BRCA1	chr8:115400344-115401027	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:115516232-115516627	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr8:115252479-115252715	HepG2	liver:	n/a	chr8:115252600-115252611
35	CEBPB	chr8:115336098-115336490	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr8:115364696-115364815	A549	lung:	n/a	chr8:115364727-115364738 chr8:115364728-115364737 chr8:115364726-115364737 chr8:115364726-115364739
37	CEBPB	chr8:115317512-115317686	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:115261940-115262622	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr8:115252438-115252677	A549	lung:	n/a	chr8:115252600-115252611
40	CEBPB	chr8:115466720-115467076	Hela-S3	cervix:	n/a	chr8:115466973-115466986
41	CEBPB	chr8:115482442-115482726	HepG2	liver:	n/a	chr8:115482612-115482623
42	CEBPB	chr8:115265592-115266087	Hela-S3	cervix:	n/a	chr8:115265672-115265683
43	CEBPB	chr8:115309955-115311248	GM12878	blood:	n/a	n/a
44	CEBPB	chr8:115265626-115265991	A549	lung:	n/a	chr8:115265672-115265683
45	CEBPB	chr8:115466783-115467017	MCF-7	breast:	n/a	chr8:115466973-115466986
46	CEBPB	chr8:115471046-115471308	HepG2	liver:	n/a	chr8:115471152-115471163
47	CEBPB	chr8:115399635-115400913	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr8:115265601-115265931	IMR90	lung:	n/a	chr8:115265672-115265683
49	CEBPB	chr8:115363238-115363247	K562	blood:	n/a	n/a
50	CEBPB	chr8:115364657-115364877	HepG2	liver:	n/a	chr8:115364727-115364738 chr8:115364728-115364737 chr8:115364726-115364737 chr8:115364726-115364739

(count:366 , 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	Jurkat	blood:	n/a
2	chr8:115493513-115493563	LNCaP	prostate:	n/a
3	chr8:115398676-115398726	HRCEpiC	kidney:	n/a
4	chr8:115516524-115516574	HCM	heart:	n/a
5	chr8:115516524-115516574	AG09309	skin:	n/a
6	chr8:115466108-115466158	HCT-116	colon:	n/a
7	chr8:115516524-115516574	CMK	blood:	n/a
8	chr8:115398676-115398726	PrEC	prostate:	n/a
9	chr8:115466108-115466158	GM06990	blood:	n/a
10	chr8:115398676-115398726	HUVEC	blood vessel:	n/a
11	chr8:115301887-115301937	NH-A	brain:	n/a
12	chr8:115516486-115516536	MCF10A-Er-Src	breast:	n/a
13	chr8:115398676-115398726	HCF	heart:	n/a
14	chr8:115516486-115516536	HEK293	kidney:	embryo
15	chr8:115516524-115516574	HCF	heart:	n/a
16	chr8:115398676-115398726	BJ	skin:	n/a
17	chr8:115466108-115466158	BE2_C	brain:	n/a
18	chr8:115516524-115516574	SAEC	small airway:	n/a
19	chr8:115398676-115398726	GM06990	blood:	n/a
20	chr8:115493513-115493563	PANC-1	pancreas:	n/a
21	chr8:115516524-115516574	MCF10A-Er-Src	breast:	n/a
22	chr8:115466108-115466158	HMEC	breast:	n/a
23	chr8:115301887-115301937	HCPEpiC	choroid plexus:	n/a
24	chr8:115301887-115301937	HUVEC	blood vessel:	n/a
25	chr8:115466108-115466158	Caco-2	colon:	n/a
26	chr8:115466108-115466158	H1-hESC	embryonic stem cell:	embryo
27	chr8:115516486-115516536	NT2-D1	testis:	n/a
28	chr8:115516524-115516574	GM06990	blood:	n/a
29	chr8:115398676-115398726	IMR90	lung:	fetal
30	chr8:115466108-115466158	AG09309	skin:	n/a
31	chr8:115493513-115493563	SK-N-SH	brain:	n/a
32	chr8:115516524-115516574	GM19239	blood:	n/a
33	chr8:115398676-115398726	ECC-1	luminal epithelium:	n/a
34	chr8:115301887-115301937	T-47D	breast:	n/a
35	chr8:115301887-115301937	HRCEpiC	kidney:	n/a
36	chr8:115301887-115301937	Hepatocyte	liver:	n/a
37	chr8:115493513-115493563	GM06990	blood:	n/a
38	chr8:115516524-115516574	HAEpiC	amniotic membrane:	n/a
39	chr8:115493513-115493563	IMR90	lung:	fetal
40	chr8:115301887-115301937	MCF10A-Er-Src	breast:	n/a
41	chr8:115516486-115516536	HIPEpiC	eye:	n/a
42	chr8:115301887-115301937	HIPEpiC	eye:	n/a
43	chr8:115516486-115516536	Hela-S3	cervix:	n/a
44	chr8:115516524-115516574	HEK293	kidney:	embryo
45	chr8:115301887-115301937	HEEpiC	esophagus:	n/a
46	chr8:115493513-115493563	HCPEpiC	choroid plexus:	n/a
47	chr8:115516524-115516574	SK-N-SH	brain:	n/a
48	chr8:115493513-115493563	AG04449	skin:	fetal
49	chr8:115493513-115493563	H1-hESC	embryonic stem cell:	embryo
50	chr8:115516524-115516574	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:115499449..115502165-chr8:115506498..115508368,2	K562	blood:
2	chr8:115501581..115504455-chr8:115510401..115513186,2	MCF-7	breast:
3	chr8:115308430..115310814-chr8:115329605..115331962,2	MCF-7	breast:
4	chr8:115313320..115315368-chr8:115318316..115320811,2	K562	blood:
5	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
6	chr8:115466661..115467320-chr8:115801108..115801704,2	MCF-7	breast:
7	chr8:115468981..115471423-chr8:115486430..115487982,2	MCF-7	breast:
8	chr8:115501581..115504455-chr8:115510401..115513186,2	MCF-7	breast:
9	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
10	chr8:115499449..115502165-chr8:115506498..115508368,2	K562	blood:
11	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:
12	chr8:115327227..115329633-chr8:115330616..115333275,2	MCF-7	breast:
13	chr5:162988387..162989071-chr8:115522859..115523605,2	HCT-116	colon:
14	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:
15	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
16	chr8:115313320..115315368-chr8:115318316..115320811,2	K562	blood:
17	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
18	chr8:115468981..115471423-chr8:115486430..115487982,2	MCF-7	breast:
19	chr17:57969212..57972136-chr8:115525975..115527526,2	MCF-7	breast:

(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	chr8:115299951-115300072	NONHSAT128356
3	lnc-CSMD3-1	chr8:115315119-115315373	XLOC_007184
4	lnc-CSMD3-1	chr8:115323322-115323497	XLOC_007184
5	lnc-CSMD3-5	chr8:115309415-115309984	NONHSAT128356
6	lnc-CSMD3-5	chr8:115308063-115308898	NONHSAT128356
7	lnc-CSMD3-1	chr8:115316636-115316724	XLOC_007184

No data

Variant related genes	Relation type
ENSG00000254339	TF binding region
ENSG00000253499	TF binding region
ENSG00000254339	CpG island
ENSG00000253499	CpG island
ENSG00000253499	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000108423	chromatin interactions
MAGT1	miRNA target sites
MAFK	miRNA target sites

Extended variants
information (count: 4708 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:4708 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1515687	chr8:115247555-115247556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570714972	chr8:115247569-115247570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529753127	chr8:115247597-115247598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572524589	chr8:115247634-115247635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541953579	chr8:115247658-115247659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199562528	chr8:115247663-115247664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563326607	chr8:115247687-115247688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191534372	chr8:115247693-115247694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539354706	chr8:115247735-115247736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539924325	chr8:115247759-115247760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114121024	chr8:115247782-115247783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542783519	chr8:115247785-115247786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79819596	chr8:115247827-115247828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148666402	chr8:115247869-115247870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184841934	chr8:115247919-115247920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528439998	chr8:115247951-115247952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546592572	chr8:115247991-115247992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142161063	chr8:115247999-115248000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35222751	chr8:115248011-115248012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554779220	chr8:115248012-115248013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189325093	chr8:115248025-115248026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192577888	chr8:115248028-115248029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35377809	chr8:115248030-115248031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569328623	chr8:115248043-115248044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555031376	chr8:115248108-115248109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79408424	chr8:115248109-115248110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148168155	chr8:115248110-115248111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573598363	chr8:115248150-115248151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78962919	chr8:115248170-115248171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552997500	chr8:115248239-115248240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs13280125	chr8:115248242-115248243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185087307	chr8:115248334-115248335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541540337	chr8:115248369-115248370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150520671	chr8:115248395-115248396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575312370	chr8:115248414-115248415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555579754	chr8:115248447-115248448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190036341	chr8:115248469-115248470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370699460	chr8:115248497-115248498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140377051	chr8:115248510-115248511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181308673	chr8:115248525-115248526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186531202	chr8:115248563-115248564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538104632	chr8:115248621-115248622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529314299	chr8:115248653-115248654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550779320	chr8:115248665-115248666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569346438	chr8:115248675-115248676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540007908	chr8:115248691-115248692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557745820	chr8:115248711-115248712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113914980	chr8:115248728-115248729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112628348	chr8:115248763-115248764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370889834	chr8:115248835-115248836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:115243200-115252800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr8:115248600-115249200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:115249000-115249600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr8:115249000-115252600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr8:115249600-115252800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:115252600-115252800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr8:115252800-115253400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr8:115252800-115253800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr8:115253000-115253600	Active TSS	Fetal Heart	heart
10	chr8:115253400-115253600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr8:115253600-115257200	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr8:115253800-115254400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr8:115254400-115255400	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr8:115254600-115255000	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr8:115254600-115255400	Active TSS	H9 Cell Line	embryonic stem cell
16	chr8:115255000-115259400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr8:115255400-115256400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr8:115255400-115259400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr8:115256400-115257200	Active TSS	H9 Cell Line	embryonic stem cell
20	chr8:115257200-115259400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr8:115259400-115259800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr8:115259400-115259800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr8:115259400-115260000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr8:115259400-115260200	Enhancers	H1 Cell Line	embryonic stem cell
25	chr8:115259400-115260200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr8:115259400-115260200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr8:115259600-115260000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr8:115259800-115260000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr8:115259800-115260400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr8:115260000-115260400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr8:115260000-115260400	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr8:115260000-115260400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr8:115260200-115269200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:115260400-115261000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr8:115260400-115261600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr8:115260400-115267200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr8:115261000-115261600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr8:115261200-115262200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr8:115261600-115262200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr8:115261800-115262000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr8:115261800-115262800	Enhancers	Hela-S3	cervix
42	chr8:115262000-115262600	Enhancers	Dnd41	blood
43	chr8:115262600-115267000	Weak transcription	Dnd41	blood
44	chr8:115267000-115267400	ZNF genes & repeats	Spleen	Spleen
45	chr8:115267000-115268000	ZNF genes & repeats	Dnd41	blood
46	chr8:115267200-115267600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
47	chr8:115267200-115267600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:115273600-115274000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr8:115277200-115277600	Enhancers	Liver	Liver
50	chr8:115278000-115278400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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