Variant report

Variant	nsv831421
Chromosome Location	chr8:110874634-111038295
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:606)
CpG islands
(count:1221)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:110977979-110978128	K562	blood:	n/a	n/a
2	BACH1	chr8:111011276-111011469	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr8:110961552-110961798	GM12878	blood:	n/a	chr8:110961773-110961780
4	BHLHE40	chr8:111010799-111010810	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:110996175-110996503	HepG2	liver:	n/a	chr8:110996318-110996329
6	CEBPB	chr8:110889129-110889322	IMR90	lung:	n/a	chr8:110889237-110889250
7	CEBPB	chr8:111034514-111034697	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:110980027-110980297	A549	lung:	n/a	n/a
9	CEBPB	chr8:110888303-110888615	A549	lung:	n/a	chr8:110888471-110888482 chr8:110888450-110888461 chr8:110888471-110888484 chr8:110888473-110888484
10	CEBPB	chr8:110888263-110888603	HepG2	liver:	n/a	chr8:110888471-110888482 chr8:110888450-110888461 chr8:110888471-110888484 chr8:110888473-110888484
11	CEBPB	chr8:110908932-110909301	H1-hESC	embryonic stem cell:	n/a	chr8:110909121-110909132
12	CEBPB	chr8:110878859-110879028	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:110977071-110977227	A549	lung:	n/a	n/a
14	CEBPB	chr8:110889155-110889282	A549	lung:	n/a	chr8:110889237-110889250
15	CEBPB	chr8:110878880-110879066	A549	lung:	n/a	n/a
16	CEBPB	chr8:110908503-110908724	A549	lung:	n/a	n/a
17	CEBPB	chr8:110909006-110909175	HepG2	liver:	n/a	chr8:110909121-110909132
18	CTBP2	chr8:110985797-110987235	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTBP2	chr8:110987468-110988080	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:110966260-110966410	GM12870	blood:	n/a	n/a
21	CTCF	chr8:110986620-110986770	HFF-Myc	foreskin:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
22	CTCF	chr8:110925263-110925271	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:110965920-110966070	HAc	cerebellar:	n/a	n/a
24	CTCF	chr8:110965980-110966130	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr8:110965640-110965790	HRE	kidney:	n/a	n/a
26	CTCF	chr8:110986680-110986830	GM12872	blood:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
27	CTCF	chr8:110986680-110986830	Caco-2	colon:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
28	CTCF	chr8:110966280-110966430	HCT-116	colon:	n/a	n/a
29	CTCF	chr8:110986627-110986899	H1-hESC	embryonic stem cell:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
30	CTCF	chr8:110986640-110986790	GM12870	blood:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
31	CTCF	chr8:110986680-110986830	HBMEC	blood vessel:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
32	CTCF	chr8:110965968-110966202	GM12878	blood:	n/a	n/a
33	CTCF	chr8:110966033-110966167	HepG2	liver:	n/a	n/a
34	CTCF	chr8:110986538-110986976	H1-hESC	embryonic stem cell:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
35	CTCF	chr8:110966000-110966150	HCFaa	heart:	n/a	n/a
36	CTCF	chr8:110966080-110966230	HAc	cerebellar:	n/a	n/a
37	CTCF	chr8:110986720-110986870	GM12867	blood:	n/a	n/a
38	CTCF	chr8:110986563-110986980	A549	lung:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
39	CTCF	chr8:110966020-110966170	Medullo	brain:	n/a	n/a
40	CTCF	chr8:110986644-110986878	Pancreas_OC	pancreas:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
41	CTCF	chr8:110986682-110986945	NHEK	skin:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
42	CTCF	chr8:110987000-110987150	RPTEC	kidney:	n/a	n/a
43	CTCF	chr8:110966040-110966190	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr8:110986673-110986927	GM12891	blood:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
45	CTCF	chr8:110966000-110966150	HL-60	blood:	n/a	n/a
46	CTCF	chr8:110986700-110986850	GM12878	blood:	n/a	chr8:110986702-110986711
47	CTCF	chr8:110986740-110986890	HAc	cerebellar:	n/a	n/a
48	CTCF	chr8:110986831-110986833	GM12878	blood:	n/a	n/a
49	CTCF	chr8:110966020-110966170	GM12865	blood:	n/a	n/a
50	CTCF	chr8:110966060-110966210	NHEK	skin:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110987781-110987831	ProgFib	skin:	n/a
2	chr8:110987781-110987831	ProgFib	skin:	n/a
3	chr8:110986371-110986421	HRPEpiC	eye:	n/a
4	chr8:110988071-110988121	HepG2	liver:	n/a
5	chr8:110986371-110986421	SAEC	small airway:	n/a
6	chr8:110987946-110987996	HRE	kidney:	n/a
7	chr8:110982709-110982759	HNPCEpiC	eye:	n/a
8	chr8:110988043-110988093	HRCEpiC	kidney:	n/a
9	chr8:110986685-110986735	SK-N-SH	brain:	n/a
10	chr8:110987530-110987580	MCF-7	breast:	n/a
11	chr8:110988444-110988494	HUVEC	blood vessel:	n/a
12	chr8:110986685-110986735	K562	blood:	n/a
13	chr8:110986974-110987024	HCF	heart:	n/a
14	chr8:110982709-110982759	NHDF-neo	bronchial:	n/a
15	chr8:110988248-110988298	NB4	blood:	n/a
16	chr8:110987530-110987580	H1-hESC	embryonic stem cell:	embryo
17	chr8:110987946-110987996	LNCaP	prostate:	n/a
18	chr8:110990365-110990415	HIPEpiC	eye:	n/a
19	chr8:110987617-110987667	PrEC	prostate:	n/a
20	chr8:110984715-110984765	HCF	heart:	n/a
21	chr8:110987946-110987996	MCF10A-Er-Src	breast:	n/a
22	chr8:110987019-110987069	HMEC	breast:	n/a
23	chr8:110986982-110987032	HCM	heart:	n/a
24	chr8:110986685-110986735	PANC-1	pancreas:	n/a
25	chr8:110987617-110987667	HEK293	kidney:	embryo
26	chr8:110988248-110988298	HAEpiC	amniotic membrane:	n/a
27	chr8:110982709-110982759	BE2_C	brain:	n/a
28	chr8:110987530-110987580	HRE	kidney:	n/a
29	chr8:110986870-110986920	A549	lung:	n/a
30	chr8:110990365-110990415	HL-60	blood:	n/a
31	chr8:110986685-110986735	HIPEpiC	eye:	n/a
32	chr8:110988043-110988093	AG09319	gingival:	n/a
33	chr8:110988444-110988494	NHBE	bronchial:	n/a
34	chr8:110987530-110987580	AoSMC	blood vessel:	n/a
35	chr8:110984715-110984765	GM12878	blood:	n/a
36	chr8:110989116-110989166	NB4	blood:	n/a
37	chr8:110986371-110986421	HCPEpiC	choroid plexus:	n/a
38	chr8:110987530-110987580	NH-A	brain:	n/a
39	chr8:110988043-110988093	PFSK-1	brain:	n/a
40	chr8:110986371-110986421	HRE	kidney:	n/a
41	chr8:110988248-110988298	GM12891	blood:	n/a
42	chr8:110987946-110987996	HMEC	breast:	n/a
43	chr8:110986982-110987032	IMR90	lung:	fetal
44	chr8:110988248-110988298	A549	lung:	n/a
45	chr8:110987530-110987580	GM12878	blood:	n/a
46	chr8:110986685-110986735	U87	brain:	n/a
47	chr8:110987530-110987580	Caco-2	colon:	n/a
48	chr8:110986685-110986735	HRPEpiC	eye:	n/a
49	chr8:110988444-110988494	GM12878	blood:	n/a
50	chr8:110987019-110987069	GM12892	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:110986569..110989011-chr8:110990714..110992570,2	K562	blood:
2	chr8:111003607..111005955-chr8:111007039..111008602,2	MCF-7	breast:
3	chr8:110345039..110348121-chr8:110985396..110989742,4	MCF-7	breast:
4	chr8:110747815..110748380-chr8:110895101..110895998,2	MCF-7	breast:
5	chr8:110981502..110984077-chr8:110985344..110987885,2	MCF-7	breast:
6	chr8:110986455..110989078-chr8:111035834..111038518,2	MCF-7	breast:
7	chr8:110965639..110966492-chr8:111038409..111038946,3	MCF-7	breast:
8	chr8:110747077..110747781-chr8:111036015..111036986,2	MCF-7	breast:
9	chr8:111011938..111014551-chr8:111015885..111018861,2	MCF-7	breast:
10	chr8:110880552..110882589-chr8:110885150..110886896,2	K562	blood:
11	chr14:42716738..42718328-chr8:110964082..110966975,2	MCF-7	breast:
12	chr8:111003607..111005955-chr8:111007039..111008602,2	MCF-7	breast:
13	chr8:111011938..111014551-chr8:111015885..111018861,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-1	chr8:110986172-110986254	ENSG00000255402.1
2	lnc-KCNV1-3	chr8:110975869-110977604	NONHSAT128306
3	lnc-KCNV1-4	chr8:110911475-110911991	NONHSAT128305
4	lnc-RP11-422N16.3.1-1	chr8:110986541-110987010	ENSG00000255402.1

No data

Variant related genes	Relation type
ENSG00000255402	TF binding region
RNU2-67P	TF binding region
ENSG00000241385	TF binding region
KCNV1	TF binding region
ENSG00000255402	CpG island
RNU2-67P	CpG island
ENSG00000241385	CpG island
KCNV1	CpG island
ENSG00000120526	chromatin interactions
ENSG00000222729	chromatin interactions
ENSG00000255402	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000164794	chromatin interactions

Extended variants
information (count: 2399 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2399 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537249113	chr8:110874665-110874666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550720512	chr8:110874669-110874670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567880979	chr8:110874670-110874671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62528038	chr8:110874683-110874684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553121469	chr8:110874729-110874730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573176668	chr8:110874730-110874731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539178653	chr8:110874800-110874801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559093357	chr8:110874842-110874843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575762799	chr8:110874853-110874854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563820615	chr8:110874854-110874855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375065241	chr8:110874856-110874857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563467883	chr8:110874871-110874872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573878688	chr8:110874872-110874873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542889626	chr8:110874896-110874897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559123423	chr8:110874941-110874942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376247820	chr8:110875129-110875130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528086041	chr8:110875154-110875155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550914533	chr8:110875157-110875158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532502885	chr8:110875189-110875190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201262869	chr8:110875193-110875194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564647742	chr8:110875194-110875195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199782624	chr8:110875198-110875199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189168046	chr8:110875218-110875219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9771971	chr8:110875223-110875224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9773507	chr8:110875224-110875225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550783996	chr8:110875246-110875247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567828083	chr8:110875258-110875259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536578733	chr8:110875285-110875286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547265957	chr8:110875323-110875324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566800819	chr8:110875326-110875327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539041492	chr8:110875331-110875332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558954254	chr8:110875338-110875339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575827890	chr8:110875342-110875343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200734644	chr8:110875355-110875356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370317749	chr8:110875377-110875378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573768106	chr8:110875385-110875386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542601771	chr8:110875392-110875393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9720918	chr8:110875398-110875399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559600943	chr8:110875400-110875401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9773536	chr8:110875410-110875411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs544620456	chr8:110875441-110875442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564513189	chr8:110875473-110875474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530548289	chr8:110875495-110875496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550635846	chr8:110875538-110875539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9773539	chr8:110875545-110875546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs56838141	chr8:110875576-110875577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546832981	chr8:110875609-110875610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567165982	chr8:110875626-110875627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532823130	chr8:110875687-110875688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552629492	chr8:110875691-110875692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
lymphocytic leukemia	21291569	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
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
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110871200-110877800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:110877400-110879200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr8:110877800-110878200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:110878200-110879000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:110878200-110879200	Enhancers	Placenta Amnion	Placenta Amnion
6	chr8:110879000-110879400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:110888800-110889200	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr8:110888800-110889200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr8:110889200-110892800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr8:110889600-110889800	Enhancers	Fetal Heart	heart
11	chr8:110890000-110891200	Weak transcription	Fetal Heart	heart
12	chr8:110891200-110892000	Enhancers	Fetal Heart	heart
13	chr8:110892000-110895800	Weak transcription	Fetal Heart	heart
14	chr8:110892800-110893600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr8:110892800-110893800	Enhancers	Duodenum Mucosa	Duodenum
16	chr8:110892800-110894600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:110893800-110896800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr8:110895800-110896800	Enhancers	Fetal Heart	heart
19	chr8:110896600-110897200	Enhancers	Fetal Brain Female	brain
20	chr8:110896800-110897800	Enhancers	Duodenum Mucosa	Duodenum
21	chr8:110897000-110897600	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr8:110897000-110897600	Enhancers	Small Intestine	intestine
23	chr8:110897200-110897600	Enhancers	Fetal Intestine Large	intestine
24	chr8:110905400-110905800	Enhancers	Fetal Brain Male	brain
25	chr8:110905800-110906800	Weak transcription	Fetal Brain Male	brain
26	chr8:110906800-110907000	Enhancers	Fetal Brain Male	brain
27	chr8:110907200-110907400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:110907600-110908600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:110908600-110909000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr8:110908600-110910400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:110908800-110909200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:110908800-110909400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:110911400-110911800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:110911400-110912000	Enhancers	Pancreas	Pancrea
35	chr8:110919000-110920600	Enhancers	Fetal Heart	heart
36	chr8:110920600-110922400	Weak transcription	Fetal Heart	heart
37	chr8:110921800-110922400	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr8:110922000-110922400	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr8:110922200-110922400	Enhancers	Pancreas	Pancrea
40	chr8:110922200-110922600	Enhancers	Fetal Brain Male	brain
41	chr8:110922400-110922600	Enhancers	Fetal Heart	heart
42	chr8:110924200-110924400	Enhancers	Fetal Brain Male	brain
43	chr8:110931400-110932200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:110931400-110932400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:110937000-110938400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr8:110937400-110937600	Enhancers	A549	lung
47	chr8:110937600-110938000	Active TSS	A549	lung
48	chr8:110938400-110940000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr8:110939400-110940000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:110939800-110940800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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