Variant report

Variant	nsv891352
Chromosome Location	chr8:115162781-115536093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1274)
CpG islands
(count:366)
Chromatin interactive
region (count:21)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1274 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:115228160-115228264	K562	blood:	n/a	n/a
2	ATF2	chr8:115309934-115311300	GM12878	blood:	n/a	n/a
3	ATF2	chr8:115524683-115525086	GM12878	blood:	n/a	n/a
4	ATF2	chr8:115524667-115525053	GM12878	blood:	n/a	n/a
5	ATF2	chr8:115310219-115310638	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:115309455-115309795	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:115309885-115311242	GM12878	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	BACH1	chr8:115441617-115441711	K562	blood:	n/a	n/a
11	BACH1	chr8:115226424-115226479	K562	blood:	n/a	n/a
12	BATF	chr8:115282793-115283090	GM12878	blood:	n/a	n/a
13	BATF	chr8:115310640-115310938	GM12878	blood:	n/a	n/a
14	BATF	chr8:115309992-115310599	GM12878	blood:	n/a	n/a
15	BATF	chr8:115318701-115318964	GM12878	blood:	n/a	chr8:115318871-115318882
16	BATF	chr8:115447401-115447735	GM12878	blood:	n/a	n/a
17	BATF	chr8:115451370-115451612	GM12878	blood:	n/a	n/a
18	BATF	chr8:115310001-115310427	GM12878	blood:	n/a	n/a
19	BATF	chr8:115447376-115447721	GM12878	blood:	n/a	n/a
20	BATF	chr8:115451366-115451632	GM12878	blood:	n/a	n/a
21	BATF	chr8:115310578-115311176	GM12878	blood:	n/a	n/a
22	BATF	chr8:115524605-115525084	GM12878	blood:	n/a	chr8:115524859-115524870
23	BATF	chr8:115281695-115281857	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:115310015-115310397	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:115310567-115311162	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:115310650-115310937	GM12878	blood:	n/a	n/a
27	BCL3	chr8:115310042-115310348	GM12878	blood:	n/a	n/a
28	BCL3	chr8:115310631-115311217	GM12878	blood:	n/a	n/a
29	BCLAF1	chr8:115310053-115311206	GM12878	blood:	n/a	n/a
30	BCLAF1	chr8:115310652-115311196	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:115281742-115281877	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:115310002-115311236	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:115282801-115283059	GM12878	blood:	n/a	n/a
34	BRCA1	chr8:115400344-115401027	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr8:115265626-115265991	A549	lung:	n/a	chr8:115265672-115265683
36	CEBPB	chr8:115182706-115183189	H1-hESC	embryonic stem cell:	n/a	chr8:115182849-115182860
37	CEBPB	chr8:115182688-115182967	HepG2	liver:	n/a	chr8:115182849-115182860
38	CEBPB	chr8:115227277-115227586	Hela-S3	cervix:	n/a	chr8:115227439-115227448 chr8:115227439-115227448 chr8:115227439-115227448 chr8:115227437-115227448 chr8:115227439-115227448 chr8:115227439-115227450
39	CEBPB	chr8:115336098-115336490	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr8:115529253-115529436	A549	lung:	n/a	n/a
41	CEBPB	chr8:115281647-115281934	HepG2	liver:	n/a	chr8:115281760-115281771
42	CEBPB	chr8:115265601-115265931	IMR90	lung:	n/a	chr8:115265672-115265683
43	CEBPB	chr8:115265560-115265854	HepG2	liver:	n/a	chr8:115265672-115265683
44	CEBPB	chr8:115261940-115262622	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr8:115471046-115471308	HepG2	liver:	n/a	chr8:115471152-115471163
46	CEBPB	chr8:115252438-115252677	A549	lung:	n/a	chr8:115252600-115252611
47	CEBPB	chr8:115227321-115227620	HepG2	liver:	n/a	chr8:115227439-115227448 chr8:115227439-115227448 chr8:115227439-115227448 chr8:115227437-115227448 chr8:115227439-115227448 chr8:115227439-115227450
48	CEBPB	chr8:115227320-115227616	K562	blood:	n/a	chr8:115227439-115227448 chr8:115227439-115227448 chr8:115227439-115227448 chr8:115227437-115227448 chr8:115227439-115227448 chr8:115227439-115227450
49	CEBPB	chr8:115529121-115529490	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr8:115364696-115364815	A549	lung:	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	HEEpiC	esophagus:	n/a
2	chr8:115398676-115398726	RPTEC	kidney:	n/a
3	chr8:115466108-115466158	GM06990	blood:	n/a
4	chr8:115466108-115466158	SAEC	small airway:	n/a
5	chr8:115516524-115516574	HCM	heart:	n/a
6	chr8:115301887-115301937	MCF-7	breast:	n/a
7	chr8:115301887-115301937	HRE	kidney:	n/a
8	chr8:115516524-115516574	HL-60	blood:	n/a
9	chr8:115301887-115301937	GM12878	blood:	n/a
10	chr8:115466108-115466158	HCT-116	colon:	n/a
11	chr8:115301887-115301937	NB4	blood:	n/a
12	chr8:115301887-115301937	AG04450	lung:	fetal
13	chr8:115493513-115493563	U87	brain:	n/a
14	chr8:115516486-115516536	GM06990	blood:	n/a
15	chr8:115516486-115516536	SK-N-SH	brain:	n/a
16	chr8:115398676-115398726	MCF10A-Er-Src	breast:	n/a
17	chr8:115516486-115516536	HRCEpiC	kidney:	n/a
18	chr8:115493513-115493563	HIPEpiC	eye:	n/a
19	chr8:115516524-115516574	U87	brain:	n/a
20	chr8:115466108-115466158	GM12892	blood:	n/a
21	chr8:115516524-115516574	GM19239	blood:	n/a
22	chr8:115398676-115398726	HEEpiC	esophagus:	n/a
23	chr8:115493513-115493563	LNCaP	prostate:	n/a
24	chr8:115516524-115516574	NH-A	brain:	n/a
25	chr8:115466108-115466158	PANC-1	pancreas:	n/a
26	chr8:115493513-115493563	Hela-S3	cervix:	n/a
27	chr8:115301887-115301937	SAEC	small airway:	n/a
28	chr8:115466108-115466158	ovcar-3	ovarian:	n/a
29	chr8:115466108-115466158	Jurkat	blood:	n/a
30	chr8:115466108-115466158	HNPCEpiC	eye:	n/a
31	chr8:115301887-115301937	K562	blood:	n/a
32	chr8:115301887-115301937	NT2-D1	testis:	n/a
33	chr8:115301887-115301937	Caco-2	colon:	n/a
34	chr8:115493513-115493563	HRCEpiC	kidney:	n/a
35	chr8:115493513-115493563	MCF10A-Er-Src	breast:	n/a
36	chr8:115301887-115301937	HCPEpiC	choroid plexus:	n/a
37	chr8:115466108-115466158	NH-A	brain:	n/a
38	chr8:115516486-115516536	ProgFib	skin:	n/a
39	chr8:115493513-115493563	HCF	heart:	n/a
40	chr8:115301887-115301937	Hepatocyte	liver:	n/a
41	chr8:115466108-115466158	HCPEpiC	choroid plexus:	n/a
42	chr8:115493513-115493563	Hepatocyte	liver:	n/a
43	chr8:115466108-115466158	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:115516486-115516536	NH-A	brain:	n/a
45	chr8:115516524-115516574	BE2_C	brain:	n/a
46	chr8:115516486-115516536	AG09309	skin:	n/a
47	chr8:115516524-115516574	BJ	skin:	n/a
48	chr8:115466108-115466158	AG09319	gingival:	n/a
49	chr8:115516524-115516574	NT2-D1	testis:	n/a
50	chr8:115301887-115301937	BJ	skin:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:115313320..115315368-chr8:115318316..115320811,2	K562	blood:
2	chr8:115466661..115467320-chr8:115801108..115801704,2	MCF-7	breast:
3	chr8:115239390..115241790-chr8:115242578..115244996,2	K562	blood:
4	chr8:115313320..115315368-chr8:115318316..115320811,2	K562	blood:
5	chr8:115327227..115329633-chr8:115330616..115333275,2	MCF-7	breast:
6	chr8:115501581..115504455-chr8:115510401..115513186,2	MCF-7	breast:
7	chr8:115468981..115471423-chr8:115486430..115487982,2	MCF-7	breast:
8	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
9	chr8:115308430..115310814-chr8:115329605..115331962,2	MCF-7	breast:
10	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:
11	chr8:115468981..115471423-chr8:115486430..115487982,2	MCF-7	breast:
12	chr8:115239390..115241790-chr8:115242578..115244996,2	K562	blood:
13	chr17:57969212..57972136-chr8:115525975..115527526,2	MCF-7	breast:
14	chr5:162988387..162989071-chr8:115522859..115523605,2	HCT-116	colon:
15	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
16	chr8:115360876..115362417-chr8:115396298..115399107,2	K562	blood:
17	chr8:115499449..115502165-chr8:115506498..115508368,2	K562	blood:
18	chr8:115501581..115504455-chr8:115510401..115513186,2	MCF-7	breast:
19	chr8:115333482..115335799-chr8:115336000..115338063,2	K562	blood:
20	chr8:115392553..115395092-chr8:115402142..115404171,2	MCF-7	breast:
21	chr8:115499449..115502165-chr8:115506498..115508368,2	K562	blood:

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

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

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: 5271 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:5271 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34095242	chr8:115182812-115182813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139720432	chr8:115182816-115182817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372065297	chr8:115182833-115182834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530074364	chr8:115182839-115182840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117053992	chr8:115182845-115182846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568217285	chr8:115182885-115182886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186376128	chr8:115182914-115182915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142977535	chr8:115182929-115182930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550299504	chr8:115182952-115182953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570178641	chr8:115182958-115182959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146142546	chr8:115182993-115182994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546625745	chr8:115183014-115183015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544170575	chr8:115183029-115183030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530253271	chr8:115183030-115183031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546775492	chr8:115183031-115183032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562856251	chr8:115183034-115183035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368437925	chr8:115183035-115183036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560586037	chr8:115183104-115183105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538748356	chr8:115183118-115183119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558751320	chr8:115183125-115183126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552116350	chr8:115183126-115183127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568831509	chr8:115183129-115183130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531478458	chr8:115183191-115183192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs137978113	chr8:115197686-115197687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528811288	chr8:115197724-115197725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548480497	chr8:115197759-115197760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562010363	chr8:115197793-115197794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116525570	chr8:115197805-115197806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547653176	chr8:115197837-115197838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570958832	chr8:115197872-115197873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189013970	chr8:115197941-115197942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191480336	chr8:115197949-115197950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534302418	chr8:115197977-115197978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116080060	chr8:115198024-115198025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374986816	chr8:115198025-115198026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554264774	chr8:115198046-115198047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535810982	chr8:115198061-115198062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555718090	chr8:115198069-115198070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149492919	chr8:115198123-115198124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534845335	chr8:115198124-115198125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557655967	chr8:115198126-115198127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184798303	chr8:115198140-115198141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144017641	chr8:115198147-115198148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563353685	chr8:115198159-115198160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577685697	chr8:115198163-115198164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573317227	chr8:115198177-115198178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529173869	chr8:115213405-115213406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552164034	chr8:115213433-115213434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570495673	chr8:115213445-115213446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569514899	chr8:115213477-115213478	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:115182800-115183200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr8:115197600-115198200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:115213400-115215000	Enhancers	Dnd41	blood
4	chr8:115223800-115225000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:115229600-115230800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:115230400-115231000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr8:115230800-115231000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:115243200-115252800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr8:115248600-115249200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:115249000-115249600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr8:115249000-115252600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr8:115249600-115252800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr8:115252600-115252800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr8:115252800-115253400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr8:115252800-115253800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr8:115253000-115253600	Active TSS	Fetal Heart	heart
17	chr8:115253400-115253600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr8:115253600-115257200	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr8:115253800-115254400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr8:115254400-115255400	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr8:115254600-115255000	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr8:115254600-115255400	Active TSS	H9 Cell Line	embryonic stem cell
23	chr8:115255000-115259400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr8:115255400-115256400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr8:115255400-115259400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr8:115256400-115257200	Active TSS	H9 Cell Line	embryonic stem cell
27	chr8:115257200-115259400	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr8:115259400-115259800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr8:115259400-115259800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr8:115259400-115260000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr8:115259400-115260200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr8:115259400-115260200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr8:115259400-115260200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:115259600-115260000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr8:115259800-115260000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr8:115259800-115260400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr8:115260000-115260400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr8:115260000-115260400	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr8:115260000-115260400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr8:115260200-115269200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr8:115260400-115261000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr8:115260400-115261600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr8:115260400-115267200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr8:115261000-115261600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr8:115261200-115262200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr8:115261600-115262200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr8:115261800-115262000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr8:115261800-115262800	Enhancers	Hela-S3	cervix
49	chr8:115262000-115262600	Enhancers	Dnd41	blood
50	chr8:115262600-115267000	Weak transcription	Dnd41	blood

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