Variant report

Variant	nsv877147
Chromosome Location	chr3:88328826-88431461
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr3:88396623-88396919	HepG2	liver:	n/a	chr3:88396754-88396765
2	CEBPB	chr3:88378808-88379094	IMR90	lung:	n/a	chr3:88378941-88378952
3	CEBPB	chr3:88396706-88396908	A549	lung:	n/a	chr3:88396754-88396765
4	CEBPB	chr3:88396713-88396914	Hela-S3	cervix:	n/a	chr3:88396754-88396765
5	CEBPB	chr3:88427165-88427365	H1-hESC	embryonic stem cell:	n/a	chr3:88427292-88427305
6	CEBPB	chr3:88378823-88378968	HepG2	liver:	n/a	chr3:88378941-88378952
7	CEBPB	chr3:88370833-88371190	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr3:88369030-88369230	A549	lung:	n/a	n/a
9	CHD1	chr3:88357026-88357066	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr3:88428300-88428450	MCF-7	breast:	n/a	chr3:88428421-88428434 chr3:88428419-88428437 chr3:88428414-88428435
11	CTCF	chr3:88383460-88383610	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr3:88366712-88366739	Gliobla	brain:	n/a	n/a
13	CTCF	chr3:88366736-88366740	GM12878	blood:	n/a	n/a
14	CTCF	chr3:88366691-88366812	HepG2	liver:	n/a	n/a
15	CTCF	chr3:88366673-88366774	MCF-7	breast:	n/a	n/a
16	CTCF	chr3:88428358-88428558	GM12878	blood:	n/a	chr3:88428421-88428434 chr3:88428419-88428437 chr3:88428414-88428435
17	CTCF	chr3:88366721-88366814	GM13977	blood:	n/a	n/a
18	CTCF	chr3:88366714-88366804	GM19238	blood:	n/a	n/a
19	CTCF	chr3:88428380-88428530	GM12865	blood:	n/a	chr3:88428421-88428434 chr3:88428419-88428437 chr3:88428414-88428435
20	CTCF	chr3:88366722-88366803	HepG2	liver:	n/a	n/a
21	CTCF	chr3:88366691-88366794	GM12892	blood:	n/a	n/a
22	CTCF	chr3:88366680-88366797	MCF-7	breast:	n/a	n/a
23	CTCF	chr3:88366675-88366780	MCF-7	breast:	n/a	n/a
24	CTCF	chr3:88366689-88366822	GM12891	blood:	n/a	n/a
25	CTCF	chr3:88366706-88366789	ProgFib	skin:	n/a	n/a
26	CTCF	chr3:88412093-88412153	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:88366639-88366827	A549	lung:	n/a	n/a
28	CTCF	chr3:88366679-88366802	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr3:88366726-88366760	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr3:88351660-88351810	GM12870	blood:	n/a	n/a
31	CTCF	chr3:88356440-88356590	AG09319	gingival:	n/a	n/a
32	CTCF	chr3:88383440-88383590	HCM	heart:	n/a	n/a
33	CTCF	chr3:88366668-88366851	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:88396440-88396590	RPTEC	kidney:	n/a	n/a
35	CTCF	chr3:88391615-88391656	HepG2	liver:	n/a	n/a
36	CTCF	chr3:88366675-88366727	GM12878	blood:	n/a	n/a
37	CTCF	chr3:88354695-88354777	LNCaP	prostate:	n/a	n/a
38	CTCF	chr3:88366660-88366810	HepG2	liver:	n/a	n/a
39	CTCF	chr3:88372984-88373041	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:88366654-88366767	MCF-7	breast:	n/a	n/a
41	E2F4	chr3:88371620-88371836	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr3:88398054-88398133	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr3:88361780-88361868	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr3:88418524-88418809	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr3:88342519-88342529	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr3:88396640-88396749	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr3:88372170-88372370	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr3:88412425-88412431	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr3:88428630-88428740	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr3:88349180-88349380	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:88352696-88352746	HCT-116	colon:	n/a
2	chr3:88352696-88352746	NHBE	bronchial:	n/a
3	chr3:88352696-88352746	ProgFib	skin:	n/a
4	chr3:88352696-88352746	HEK293	kidney:	embryo
5	chr3:88352696-88352746	HNPCEpiC	eye:	n/a
6	chr3:88352696-88352746	SKMC	muscle:	n/a
7	chr3:88352696-88352746	ECC-1	luminal epithelium:	n/a
8	chr3:88352696-88352746	AoSMC	blood vessel:	n/a
9	chr3:88352696-88352746	PANC-1	pancreas:	n/a
10	chr3:88352696-88352746	Jurkat	blood:	n/a
11	chr3:88352696-88352746	HIPEpiC	eye:	n/a
12	chr3:88352696-88352746	ovcar-3	ovarian:	n/a
13	chr3:88352696-88352746	GM12891	blood:	n/a
14	chr3:88352696-88352746	CMK	blood:	n/a
15	chr3:88352696-88352746	AG09309	skin:	n/a
16	chr3:88352696-88352746	HRE	kidney:	n/a
17	chr3:88352696-88352746	NHDF-neo	bronchial:	n/a
18	chr3:88352696-88352746	Hela-S3	cervix:	n/a
19	chr3:88352696-88352746	HMEC	breast:	n/a
20	chr3:88352696-88352746	HRPEpiC	eye:	n/a
21	chr3:88352696-88352746	HCM	heart:	n/a
22	chr3:88352696-88352746	A549	lung:	n/a
23	chr3:88352696-88352746	HL-60	blood:	n/a
24	chr3:88352696-88352746	IMR90	lung:	fetal
25	chr3:88352696-88352746	Hepatocyte	liver:	n/a
26	chr3:88352696-88352746	SAEC	small airway:	n/a
27	chr3:88352696-88352746	SK-N-SH_RA	brain:	n/a
28	chr3:88352696-88352746	GM06990	blood:	n/a
29	chr3:88352696-88352746	HEEpiC	esophagus:	n/a
30	chr3:88352696-88352746	MCF10A-Er-Src	breast:	n/a
31	chr3:88352696-88352746	GM12892	blood:	n/a
32	chr3:88352696-88352746	GM12878	blood:	n/a
33	chr3:88352696-88352746	BE2_C	brain:	n/a
34	chr3:88352696-88352746	HepG2	liver:	n/a
35	chr3:88352696-88352746	PFSK-1	brain:	n/a
36	chr3:88352696-88352746	HUVEC	blood vessel:	n/a
37	chr3:88352696-88352746	AG04450	lung:	fetal
38	chr3:88352696-88352746	AG09319	gingival:	n/a
39	chr3:88352696-88352746	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:88352696-88352746	K562	blood:	n/a
41	chr3:88352696-88352746	PrEC	prostate:	n/a
42	chr3:88352696-88352746	HCPEpiC	choroid plexus:	n/a
43	chr3:88352696-88352746	AG10803	skin:	n/a
44	chr3:88352696-88352746	Caco-2	colon:	n/a
45	chr3:88352696-88352746	SK-N-SH	brain:	n/a
46	chr3:88352696-88352746	SK-N-MC	brain:	n/a
47	chr3:88352696-88352746	U87	brain:	n/a
48	chr3:88352696-88352746	MCF-7	breast:	n/a
49	chr3:88352696-88352746	NB4	blood:	n/a
50	chr3:88352696-88352746	AG04449	skin:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:88377277..88378950-chr3:88387834..88390220,2	MCF-7	breast:
2	chr3:88377277..88378950-chr3:88387834..88390220,2	MCF-7	breast:
3	chr3:88348034..88350434-chr3:88355298..88358101,2	MCF-7	breast:
4	chr3:88356773..88358838-chr3:88359447..88361325,2	K562	blood:
5	chr3:88356773..88358838-chr3:88359447..88361325,2	K562	blood:
6	chr3:88348034..88350434-chr3:88355298..88358101,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf38-2	chr3:88387572-88387793	NONHSAT090703
2	lnc-C3orf38-2	chr3:88387573-88387793	XLOC_002727
3	lnc-C3orf38-2	chr3:88387591-88387793	XLOC_002727
4	lnc-C3orf38-2	chr3:88392302-88392435	XLOC_002727
5	lnc-C3orf38-2	chr3:88387573-88387793	XLOC_002727
6	lnc-C3orf38-2	chr3:88418571-88418634	XLOC_002727
7	lnc-C3orf38-2	chr3:88392301-88392435	NONHSAT090703

No data

Variant related genes	Relation type
ABCF2P1	TF binding region
ABCF2P1	CpG island
BLCAP	miRNA target sites
E2F8	miRNA target sites
VLDLR	miRNA target sites

Extended variants
information (count: 1423 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1423 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567638678	chr3:88330623-88330624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs199665739	chr3:88330657-88330658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147297022	chr3:88330694-88330695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113367902	chr3:88330703-88330704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189560349	chr3:88330748-88330749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140958301	chr3:88330773-88330774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181619311	chr3:88330821-88330822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536200183	chr3:88330825-88330826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533843414	chr3:88330873-88330874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568933871	chr3:88330883-88330884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554602231	chr3:88330922-88330923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111388579	chr3:88330958-88330959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572776328	chr3:88331014-88331015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs56808168	chr3:88331028-88331029	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs367821395	chr3:88331030-88331031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543528109	chr3:88331038-88331039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371390041	chr3:88331067-88331068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375668381	chr3:88331078-88331079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10549387	chr3:88331079-88331080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375805943	chr3:88331080-88331081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376796996	chr3:88331092-88331093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543958443	chr3:88331106-88331107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78192692	chr3:88331123-88331124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369844260	chr3:88331126-88331127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375468511	chr3:88331145-88331146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576939518	chr3:88331218-88331219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530949637	chr3:88331228-88331229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9858848	chr3:88331267-88331268	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs540882639	chr3:88331273-88331274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141565509	chr3:88331294-88331295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186799381	chr3:88331346-88331347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546992243	chr3:88331347-88331348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571880569	chr3:88331366-88331367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191390930	chr3:88331407-88331408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559557200	chr3:88331439-88331440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529947218	chr3:88331441-88331442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150911435	chr3:88331448-88331449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569470275	chr3:88331472-88331473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375101593	chr3:88331481-88331482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553731260	chr3:88331554-88331555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541767031	chr3:88331636-88331637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563330000	chr3:88331640-88331641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181461153	chr3:88331654-88331655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139234268	chr3:88331708-88331709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576683481	chr3:88331741-88331742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184996554	chr3:88331746-88331747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555983494	chr3:88331765-88331766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113625695	chr3:88331786-88331787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542787892	chr3:88331790-88331791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116078232	chr3:88331801-88331802	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22522925	CNVD
Lung cancer	19547694	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:88330600-88332200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr3:88332200-88332400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:88332200-88333000	Enhancers	Ovary	ovary
4	chr3:88332200-88333600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:88332400-88339800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:88333000-88334000	Weak transcription	Ovary	ovary
7	chr3:88333600-88334400	Enhancers	Small Intestine	intestine
8	chr3:88333800-88334000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:88334200-88334400	Enhancers	Ovary	ovary
10	chr3:88339800-88342000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:88340400-88341200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:88340600-88341000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr3:88341200-88342000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr3:88347000-88347200	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr3:88347200-88347600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
16	chr3:88347200-88348000	Enhancers	Primary T cells from cord blood	blood
17	chr3:88347400-88347800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:88347600-88347800	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr3:88347800-88348000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
20	chr3:88347800-88350000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr3:88348000-88348600	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr3:88348600-88350000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr3:88350000-88351000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr3:88350000-88352000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:88351000-88358600	Weak transcription	Right Atrium	heart
26	chr3:88352200-88352800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:88355200-88360000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr3:88355400-88357400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr3:88355600-88357000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr3:88355600-88359000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr3:88355600-88359800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr3:88355800-88359400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr3:88356000-88356200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr3:88356000-88356200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr3:88356200-88356800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr3:88356200-88358400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr3:88356800-88357000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:88356800-88357200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:88356800-88357200	Enhancers	Brain Germinal Matrix	brain
40	chr3:88356800-88357200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr3:88356800-88357200	Enhancers	Pancreas	Pancrea
42	chr3:88356800-88357600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr3:88357000-88357200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:88357000-88357400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr3:88357000-88357800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr3:88357400-88358000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr3:88357400-88358800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr3:88358000-88359000	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr3:88358400-88359200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr3:88359000-88361000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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