Variant report

Variant	nsv1033792
Chromosome Location	chr8:111824536-111906864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1024)
CpG islands
(count:366)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:111842727-111843064	K562	blood:	n/a	n/a
2	ARID3A	chr8:111842737-111843081	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:111844737-111844834	K562	blood:	n/a	n/a
4	ARID3A	chr8:111860419-111860636	K562	blood:	n/a	n/a
5	ARID3A	chr8:111861128-111861289	K562	blood:	n/a	n/a
6	ARID3A	chr8:111844706-111844955	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:111860272-111860903	HepG2	liver:	n/a	chr8:111860332-111860348
8	ATF1	chr8:111875900-111876067	K562	blood:	n/a	n/a
9	ATF1	chr8:111906691-111907234	K562	blood:	n/a	n/a
10	ATF3	chr8:111860291-111860669	K562	blood:	n/a	n/a
11	BATF	chr8:111860419-111860570	GM12878	blood:	n/a	chr8:111860544-111860554
12	BATF	chr8:111887241-111887473	GM12878	blood:	n/a	chr8:111887372-111887383 chr8:111887369-111887379 chr8:111887386-111887397
13	BATF	chr8:111887230-111887546	GM12878	blood:	n/a	chr8:111887372-111887383 chr8:111887369-111887379 chr8:111887386-111887397
14	BHLHE40	chr8:111906788-111907219	K562	blood:	n/a	n/a
15	BHLHE40	chr8:111842552-111842735	K562	blood:	n/a	n/a
16	BRCA1	chr8:111906219-111906223	HepG2	liver:	n/a	n/a
17	BRCA1	chr8:111846598-111846609	HepG2	liver:	n/a	n/a
18	BRCA1	chr8:111880545-111880672	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr8:111906683-111907203	K562	blood:	n/a	n/a
20	CCNT2	chr8:111906640-111907232	K562	blood:	n/a	n/a
21	CEBPB	chr8:111901900-111902055	HepG2	liver:	n/a	chr8:111901958-111901967 chr8:111901958-111901967 chr8:111901958-111901969 chr8:111901958-111901967 chr8:111901956-111901967 chr8:111901956-111901969 chr8:111901958-111901967 chr8:111901956-111901969
22	CEBPB	chr8:111867670-111867880	MCF-7	breast:	n/a	chr8:111867774-111867785
23	CEBPB	chr8:111867668-111867906	HepG2	liver:	n/a	chr8:111867774-111867785
24	CEBPB	chr8:111847032-111847354	IMR90	lung:	n/a	n/a
25	CEBPB	chr8:111856388-111856588	HepG2	liver:	n/a	chr8:111856520-111856532
26	CEBPB	chr8:111856639-111856677	K562	blood:	n/a	n/a
27	CEBPB	chr8:111856485-111856584	A549	lung:	n/a	chr8:111856520-111856532
28	CEBPB	chr8:111876958-111877212	K562	blood:	n/a	n/a
29	CEBPB	chr8:111891776-111891974	A549	lung:	n/a	n/a
30	CEBPB	chr8:111901847-111902044	A549	lung:	n/a	chr8:111901958-111901967 chr8:111901958-111901967 chr8:111901958-111901969 chr8:111901958-111901967 chr8:111901956-111901967 chr8:111901956-111901969 chr8:111901958-111901967 chr8:111901956-111901969
31	CHD2	chr8:111847633-111848502	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr8:111872571-111872576	HepG2	liver:	n/a	n/a
33	CREB1	chr8:111847735-111848094	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr8:111842860-111843010	WI-38	lung:	n/a	chr8:111842889-111842910 chr8:111842887-111842905 chr8:111842888-111842904
35	CTCF	chr8:111834380-111834530	GM12870	blood:	n/a	n/a
36	CTCF	chr8:111834420-111834570	BE2_C	brain:	n/a	n/a
37	CTCF	chr8:111842520-111842670	GM12873	blood:	n/a	n/a
38	CTCF	chr8:111834420-111834570	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr8:111834400-111834550	GM12875	blood:	n/a	n/a
40	CTCF	chr8:111842700-111842850	HAc	cerebellar:	n/a	n/a
41	CTCF	chr8:111906859-111906894	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr8:111844840-111844990	GM12868	blood:	n/a	n/a
43	CTCF	chr8:111848420-111848570	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr8:111842800-111842950	NHDF-neo	bronchial:	n/a	chr8:111842889-111842910 chr8:111842887-111842905 chr8:111842888-111842904
45	CTCF	chr8:111842797-111842965	HepG2	liver:	n/a	chr8:111842889-111842910 chr8:111842887-111842905 chr8:111842888-111842904
46	CTCF	chr8:111842400-111842550	GM12870	blood:	n/a	n/a
47	CTCF	chr8:111848520-111848670	HAc	cerebellar:	n/a	n/a
48	CTCF	chr8:111834378-111834753	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:111834306-111834724	A549	lung:	n/a	n/a
50	CTCF	chr8:111842820-111842970	Caco-2	colon:	n/a	chr8:111842889-111842910 chr8:111842887-111842905 chr8:111842888-111842904

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111834906-111834956	HMEC	breast:	n/a
2	chr8:111906503-111906553	BJ	skin:	n/a
3	chr8:111834752-111834802	Hela-S3	cervix:	n/a
4	chr8:111847388-111847438	CMK	blood:	n/a
5	chr8:111834776-111834826	NB4	blood:	n/a
6	chr8:111834752-111834802	HIPEpiC	eye:	n/a
7	chr8:111906503-111906553	HRCEpiC	kidney:	n/a
8	chr8:111847388-111847438	AG09309	skin:	n/a
9	chr8:111834776-111834826	IMR90	lung:	fetal
10	chr8:111834752-111834802	AG04449	skin:	fetal
11	chr8:111834906-111834956	T-47D	breast:	n/a
12	chr8:111834752-111834802	BE2_C	brain:	n/a
13	chr8:111835043-111835093	CMK	blood:	n/a
14	chr8:111906503-111906553	Caco-2	colon:	n/a
15	chr8:111834776-111834826	ECC-1	luminal epithelium:	n/a
16	chr8:111835043-111835093	LNCaP	prostate:	n/a
17	chr8:111834906-111834956	HEK293	kidney:	embryo
18	chr8:111834906-111834956	GM12891	blood:	n/a
19	chr8:111906503-111906553	GM19239	blood:	n/a
20	chr8:111906503-111906553	HEEpiC	esophagus:	n/a
21	chr8:111847388-111847438	NH-A	brain:	n/a
22	chr8:111834776-111834826	BJ	skin:	n/a
23	chr8:111835043-111835093	Hepatocyte	liver:	n/a
24	chr8:111835043-111835093	SK-N-SH_RA	brain:	n/a
25	chr8:111834776-111834826	NHBE	bronchial:	n/a
26	chr8:111847388-111847438	Hela-S3	cervix:	n/a
27	chr8:111906503-111906553	AoSMC	blood vessel:	n/a
28	chr8:111834776-111834826	GM06990	blood:	n/a
29	chr8:111847388-111847438	HRE	kidney:	n/a
30	chr8:111835043-111835093	RPTEC	kidney:	n/a
31	chr8:111834752-111834802	SK-N-SH_RA	brain:	n/a
32	chr8:111834906-111834956	Caco-2	colon:	n/a
33	chr8:111834776-111834826	HEEpiC	esophagus:	n/a
34	chr8:111906503-111906553	AG09319	gingival:	n/a
35	chr8:111847388-111847438	SK-N-SH_RA	brain:	n/a
36	chr8:111906503-111906553	MCF-7	breast:	n/a
37	chr8:111847388-111847438	BE2_C	brain:	n/a
38	chr8:111834776-111834826	HNPCEpiC	eye:	n/a
39	chr8:111834776-111834826	Hela-S3	cervix:	n/a
40	chr8:111834776-111834826	NT2-D1	testis:	n/a
41	chr8:111834752-111834802	ProgFib	skin:	n/a
42	chr8:111834906-111834956	AG09309	skin:	n/a
43	chr8:111906503-111906553	ProgFib	skin:	n/a
44	chr8:111834906-111834956	A549	lung:	n/a
45	chr8:111834752-111834802	HCF	heart:	n/a
46	chr8:111834752-111834802	CMK	blood:	n/a
47	chr8:111834906-111834956	SK-N-SH_RA	brain:	n/a
48	chr8:111847388-111847438	Hepatocyte	liver:	n/a
49	chr8:111906503-111906553	HCPEpiC	choroid plexus:	n/a
50	chr8:111834906-111834956	SKMC	muscle:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:111855787..111857322-chr8:111859376..111860898,2	MCF-7	breast:
2	chr8:111853597..111856569-chr8:111856769..111860452,3	MCF-7	breast:
3	chr8:111905656..111907856-chr8:111909688..111913737,4	K562	blood:
4	chr8:111906809..111908563-chr8:111915252..111917279,2	K562	blood:
5	chr8:111877803..111878676-chr8:112126153..112126932,3	MCF-7	breast:
6	chr17:77766844..77769049-chr8:111860348..111862470,2	MCF-7	breast:
7	chr8:111059646..111060573-chr8:111844351..111844977,3	MCF-7	breast:
8	chr8:111853597..111856569-chr8:111856769..111860452,3	MCF-7	breast:
9	chr8:111855787..111857322-chr8:111859376..111860898,2	MCF-7	breast:
10	chr8:111365378..111366118-chr8:111834050..111834594,2	MCF-7	breast:
11	chr8:110746955..110747968-chr8:111842364..111843455,3	MCF-7	breast:
12	chr8:111877803..111878653-chr8:112126153..112126716,2	MCF-7	breast:
13	chr8:111365137..111367407-chr8:111844337..111845381,8	MCF-7	breast:
14	chr8:111668947..111669607-chr8:111877933..111878646,3	MCF-7	breast:
15	chr8:111842460..111843306-chr8:121617683..121618475,2	MCF-7	breast:
16	chr8:111148225..111150967-chr8:111837407..111839836,2	MCF-7	breast:
17	chr8:111059529..111060611-chr8:111844370..111845275,3	MCF-7	breast:
18	chr8:111811884..111813878-chr8:111822855..111824615,2	K562	blood:
19	chr8:111870941..111873511-chr8:111873961..111876570,2	K562	blood:
20	chr8:111846862..111847654-chr8:112265014..112265719,2	MCF-7	breast:
21	chr8:111365308..111365953-chr8:111842805..111843518,2	MCF-7	breast:
22	chr8:111905363..111907255-chr8:112045592..112048412,2	K562	blood:
23	chr1:225202258..225204234-chr8:111898982..111900583,2	MCF-7	breast:
24	chr8:111842914..111844843-chr8:111916183..111918986,2	MCF-7	breast:
25	chr8:111870941..111873511-chr8:111873961..111876570,2	K562	blood:
26	chr8:111877768..111878423-chr8:111945734..111946406,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253994	TF binding region
ENSG00000253994	CpG island

Extended variants
information (count: 1743 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1743 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191401214	chr8:111824542-111824543	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs62526919	chr8:111824551-111824552	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs368621233	chr8:111824619-111824620	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs184151561	chr8:111824657-111824658	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs148196004	chr8:111824667-111824668	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs557885061	chr8:111824710-111824711	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs537072875	chr8:111824732-111824733	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558878172	chr8:111824742-111824743	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs369854414	chr8:111824766-111824767	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs73319770	chr8:111824777-111824778	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs207469668	chr8:111824799-111824800	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs571546887	chr8:111824822-111824823	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs543557881	chr8:111824844-111824845	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs548905455	chr8:111824856-111824857	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557093070	chr8:111824869-111824870	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs534118201	chr8:111824892-111824893	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs73319771	chr8:111824939-111824940	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs567394735	chr8:111824968-111824969	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs542862214	chr8:111825010-111825011	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs559597961	chr8:111825089-111825090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs16881058	chr8:111825127-111825128	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs16881060	chr8:111825185-111825186	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs187055593	chr8:111825271-111825272	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs530579647	chr8:111825317-111825318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190977278	chr8:111825378-111825379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561003675	chr8:111825405-111825406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7357463	chr8:111825453-111825454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182398788	chr8:111825464-111825465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372309023	chr8:111825469-111825470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546842117	chr8:111825527-111825528	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs566727539	chr8:111825567-111825568	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs538580531	chr8:111825581-111825582	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs551709598	chr8:111825607-111825608	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs571562824	chr8:111825616-111825617	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs186787294	chr8:111825630-111825631	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs374024796	chr8:111825644-111825645	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs569022954	chr8:111825671-111825672	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs573826322	chr8:111825703-111825704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191911959	chr8:111825743-111825744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7357465	chr8:111825764-111825765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6996359	chr8:111825791-111825792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573454648	chr8:111825811-111825812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114702676	chr8:111825812-111825813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6996649	chr8:111825821-111825822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs368929985	chr8:111825822-111825823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144035830	chr8:111825831-111825832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182806489	chr8:111825877-111825878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188666706	chr8:111825887-111825888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7000389	chr8:111825889-111825890	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs530808370	chr8:111825918-111825919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Glioblastoma multiforme	21080181	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
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
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111788600-111826200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:111826200-111826400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:111834600-111835000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:111835000-111842600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:111839600-111839800	Enhancers	H9 Cell Line	embryonic stem cell
6	chr8:111840000-111840400	Enhancers	Fetal Lung	lung
7	chr8:111840400-111847200	Weak transcription	Fetal Lung	lung
8	chr8:111841800-111842200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr8:111841800-111842400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr8:111841800-111842600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr8:111841800-111842800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr8:111841800-111842800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr8:111842000-111842200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:111842000-111842600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:111842000-111842600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:111842000-111842800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:111842000-111842800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:111842200-111842600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr8:111842200-111847000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr8:111842200-111847200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr8:111842400-111842600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr8:111842400-111842600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr8:111842600-111842800	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr8:111842600-111844000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr8:111842600-111844400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr8:111842600-111847200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr8:111842600-111848200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr8:111842800-111843600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr8:111842800-111843800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr8:111842800-111844000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr8:111842800-111846800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr8:111842800-111847200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:111843600-111845200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr8:111843800-111844400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:111843800-111845200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:111844000-111844400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr8:111844000-111844600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr8:111844400-111845200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr8:111844400-111846200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:111844400-111847200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr8:111844600-111847400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr8:111845200-111846600	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr8:111845200-111847000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr8:111845200-111847000	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr8:111845400-111846200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr8:111845800-111846600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr8:111846200-111847000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:111846200-111847200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr8:111846600-111847600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:111846600-111849400	Enhancers	HUES64 Cell Line	embryonic stem cell

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