Variant report

Variant	nsv834759
Chromosome Location	chr3:88901229-89105366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr3:88986169-88986369	K562	blood:	n/a	n/a
2	CEBPB	chr3:89081532-89081767	ECC-1	luminal epithelium:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
3	CEBPB	chr3:89074310-89074735	ECC-1	luminal epithelium:	n/a	chr3:89074330-89074343 chr3:89074332-89074343 chr3:89074330-89074343 chr3:89074332-89074343
4	CEBPB	chr3:89070832-89071184	IMR90	lung:	n/a	n/a
5	CEBPB	chr3:88991573-88991889	A549	lung:	n/a	chr3:88991714-88991725
6	CEBPB	chr3:89049823-89050345	Hela-S3	cervix:	n/a	chr3:89049911-89049924 chr3:89050186-89050199 chr3:89050186-89050197
7	CEBPB	chr3:89001206-89001427	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr3:89051379-89051704	IMR90	lung:	n/a	n/a
9	CEBPB	chr3:88991571-88991883	HepG2	liver:	n/a	chr3:88991714-88991725
10	CEBPB	chr3:89051407-89051635	A549	lung:	n/a	n/a
11	CEBPB	chr3:89051438-89051681	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:89099791-89099870	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:89088062-89088315	Hela-S3	cervix:	n/a	chr3:89088215-89088226
14	CEBPB	chr3:89088054-89088386	H1-hESC	embryonic stem cell:	n/a	chr3:89088215-89088226
15	CEBPB	chr3:88944385-88944631	A549	lung:	n/a	chr3:88944520-88944531 chr3:88944520-88944529 chr3:88944518-88944529 chr3:88944520-88944529 chr3:88944518-88944531 chr3:88944520-88944529 chr3:88944520-88944529 chr3:88944518-88944531
16	CEBPB	chr3:89001120-89001467	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:89074405-89074757	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr3:88961349-88961808	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr3:89074376-89074717	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:89081560-89081809	HepG2	liver:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
21	CEBPB	chr3:89088051-89088408	IMR90	lung:	n/a	chr3:89088215-89088226
22	CEBPB	chr3:89034553-89034901	IMR90	lung:	n/a	chr3:89034706-89034717
23	CEBPB	chr3:89088037-89088393	HepG2	liver:	n/a	chr3:89088215-89088226
24	CEBPB	chr3:89037926-89038148	HepG2	liver:	n/a	chr3:89038034-89038045
25	CEBPB	chr3:89081525-89081839	IMR90	lung:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
26	CEBPB	chr3:88991580-88991896	IMR90	lung:	n/a	chr3:88991714-88991725
27	CEBPB	chr3:89096183-89096427	HepG2	liver:	n/a	chr3:89096325-89096342
28	CEBPB	chr3:89088103-89088358	A549	lung:	n/a	chr3:89088215-89088226
29	CEBPB	chr3:88956651-88956824	HepG2	liver:	n/a	chr3:88956725-88956738 chr3:88956726-88956737
30	CEBPB	chr3:89034569-89034769	H1-hESC	embryonic stem cell:	n/a	chr3:89034706-89034717
31	CEBPB	chr3:88985956-88986262	HepG2	liver:	n/a	chr3:88986086-88986097
32	CEBPB	chr3:89034609-89034859	A549	lung:	n/a	chr3:89034706-89034717
33	CEBPB	chr3:88944408-88944664	HepG2	liver:	n/a	chr3:88944520-88944531 chr3:88944520-88944529 chr3:88944518-88944529 chr3:88944520-88944529 chr3:88944518-88944531 chr3:88944520-88944529 chr3:88944520-88944529 chr3:88944518-88944531
34	CHD2	chr3:88961338-88961903	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr3:89098360-89098510	GM12870	blood:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
36	CTCF	chr3:89098440-89098590	AG09309	skin:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
37	CTCF	chr3:89098380-89098530	GM12865	blood:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
38	CTCF	chr3:89041740-89041890	NHEK	skin:	n/a	n/a
39	CTCF	chr3:89098340-89098490	HEK293	kidney:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
40	CTCF	chr3:89098380-89098530	AoAF	blood vessel:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
41	CTCF	chr3:89041740-89041890	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr3:89098320-89098470	HA-sp	spinal cord:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
43	CTCF	chr3:89098350-89098542	HepG2	liver:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
44	CTCF	chr3:89098320-89098470	HRE	kidney:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
45	CTCF	chr3:89098380-89098530	GM12868	blood:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
46	CTCF	chr3:89098380-89098530	HFF-Myc	foreskin:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
47	CTCF	chr3:89098416-89098420	GM19239	blood:	n/a	n/a
48	CTCF	chr3:88953239-88953312	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr3:89098320-89098470	NHDF-neo	bronchial:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
50	CTCF	chr3:89098227-89098613	H1-hESC	embryonic stem cell:	n/a	chr3:89098447-89098456 chr3:89098441-89098459

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:88961910-88961960	AG04449	skin:	fetal
2	chr3:88961910-88961960	GM12892	blood:	n/a
3	chr3:88961910-88961960	HAEpiC	amniotic membrane:	n/a
4	chr3:88961910-88961960	HRPEpiC	eye:	n/a
5	chr3:88961910-88961960	K562	blood:	n/a
6	chr3:89097455-89097505	HRE	kidney:	n/a
7	chr3:89097455-89097505	BJ	skin:	n/a
8	chr3:89097455-89097505	PANC-1	pancreas:	n/a
9	chr3:89097455-89097505	AoSMC	blood vessel:	n/a
10	chr3:89097455-89097505	HRCEpiC	kidney:	n/a
11	chr3:88961910-88961960	HepG2	liver:	n/a
12	chr3:88961910-88961960	AG10803	skin:	n/a
13	chr3:89097455-89097505	AG10803	skin:	n/a
14	chr3:89097455-89097505	HL-60	blood:	n/a
15	chr3:88961910-88961960	PFSK-1	brain:	n/a
16	chr3:89097455-89097505	HepG2	liver:	n/a
17	chr3:88961910-88961960	RPTEC	kidney:	n/a
18	chr3:88961910-88961960	SAEC	small airway:	n/a
19	chr3:89097455-89097505	IMR90	lung:	fetal
20	chr3:88961910-88961960	GM12891	blood:	n/a
21	chr3:89097455-89097505	Hela-S3	cervix:	n/a
22	chr3:89097455-89097505	GM12892	blood:	n/a
23	chr3:88961910-88961960	BE2_C	brain:	n/a
24	chr3:89097455-89097505	HEK293	kidney:	embryo
25	chr3:89097455-89097505	MCF10A-Er-Src	breast:	n/a
26	chr3:88961910-88961960	SKMC	muscle:	n/a
27	chr3:88961910-88961960	BJ	skin:	n/a
28	chr3:88961910-88961960	Jurkat	blood:	n/a
29	chr3:88961910-88961960	GM06990	blood:	n/a
30	chr3:88961910-88961960	NH-A	brain:	n/a
31	chr3:89097455-89097505	NT2-D1	testis:	n/a
32	chr3:88961910-88961960	HIPEpiC	eye:	n/a
33	chr3:89097455-89097505	BE2_C	brain:	n/a
34	chr3:88961910-88961960	MCF-7	breast:	n/a
35	chr3:89097455-89097505	ProgFib	skin:	n/a
36	chr3:88961910-88961960	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:88961910-88961960	NT2-D1	testis:	n/a
38	chr3:88961910-88961960	HCM	heart:	n/a
39	chr3:89097455-89097505	HMEC	breast:	n/a
40	chr3:89097455-89097505	AG09309	skin:	n/a
41	chr3:88961910-88961960	LNCaP	prostate:	n/a
42	chr3:89097455-89097505	HCT-116	colon:	n/a
43	chr3:88961910-88961960	NB4	blood:	n/a
44	chr3:88961910-88961960	PrEC	prostate:	n/a
45	chr3:89097455-89097505	RPTEC	kidney:	n/a
46	chr3:89097455-89097505	AG04449	skin:	fetal
47	chr3:88961910-88961960	ovcar-3	ovarian:	n/a
48	chr3:88961910-88961960	T-47D	breast:	n/a
49	chr3:88961910-88961960	ECC-1	luminal epithelium:	n/a
50	chr3:88961910-88961960	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:57914823..57917148-chr3:89056739..89059275,2	MCF-7	breast:
2	chr3:88961750..88964041-chr3:88967426..88970423,2	MCF-7	breast:
3	chr3:88961750..88964041-chr3:88967426..88970423,2	MCF-7	breast:
4	chr3:89005246..89007637-chr7:93973935..93976038,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGGBP1-2	chr3:89096592-89097584	NONHSAT090710

Variant related genes	Relation type
GAPDHP50	TF binding region
NARG2P2	TF binding region
GAPDHP50	CpG island
NARG2P2	CpG island
ENSG00000062716	chromatin interactions

Extended variants
information (count: 3910 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3910 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528616239	chr3:88912022-88912023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140719366	chr3:88912037-88912038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs180916265	chr3:88912068-88912069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532888826	chr3:88912081-88912082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs28523924	chr3:88912087-88912088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1483485	chr3:88912109-88912110	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs569271786	chr3:88912127-88912128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530985461	chr3:88912150-88912151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552098706	chr3:88912206-88912207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74719788	chr3:88912250-88912251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563885468	chr3:88912267-88912268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4301012	chr3:88912283-88912284	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs35316336	chr3:88912286-88912287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546689240	chr3:88912305-88912306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1483486	chr3:88912331-88912332	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs558761508	chr3:88912374-88912375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577039670	chr3:88912405-88912406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184608542	chr3:88912427-88912428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373694939	chr3:88912442-88912443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556199102	chr3:88912443-88912444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574345751	chr3:88912452-88912453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541428824	chr3:88912457-88912458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149791758	chr3:88912460-88912461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527425772	chr3:88912469-88912470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565360563	chr3:88912479-88912480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527917384	chr3:88912491-88912492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190755243	chr3:88912502-88912503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548028624	chr3:88912517-88912518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373368493	chr3:88912525-88912526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565504839	chr3:88912589-88912590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1483487	chr3:88912601-88912602	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs181680433	chr3:88912649-88912650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187136042	chr3:88912653-88912654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144742329	chr3:88912659-88912660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548640227	chr3:88912687-88912688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530421025	chr3:88912711-88912712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566966618	chr3:88912770-88912771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs72929836	chr3:88912812-88912813	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs569078478	chr3:88912868-88912869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570589856	chr3:88912882-88912883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550905986	chr3:88912911-88912912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556376214	chr3:88912919-88912920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539305567	chr3:88912948-88912949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574402304	chr3:88912980-88912981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535073733	chr3:88913005-88913006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191170605	chr3:88913073-88913074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571788459	chr3:88913151-88913152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528580029	chr3:88913172-88913173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs199829479	chr3:88913173-88913174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs199677359	chr3:88913182-88913183	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Lung cancer	19547694	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	19651600	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:88912000-88913200	Enhancers	Osteobl	bone
2	chr3:88912200-88913000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr3:88912200-88913000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr3:88912600-88913000	Enhancers	NH-A	brain
5	chr3:88917400-88917800	Enhancers	Fetal Heart	heart
6	chr3:88925800-88926200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr3:88925800-88926200	Enhancers	HMEC	breast
8	chr3:88925800-88926400	Enhancers	NHEK	skin
9	chr3:88926200-88928800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:88926200-88928800	Weak transcription	HMEC	breast
11	chr3:88926400-88928600	Weak transcription	NHEK	skin
12	chr3:88928600-88929200	Enhancers	NHEK	skin
13	chr3:88928800-88929200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:88928800-88929400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr3:88928800-88929400	Enhancers	HMEC	breast
16	chr3:88945000-88945200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr3:88946400-88946600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr3:88946600-88947200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:88946600-88947200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr3:88946800-88947400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr3:88947400-88948400	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr3:88948400-88948600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr3:88958600-88958800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr3:88958800-88959000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr3:88958800-88961200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:88959000-88959800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr3:88959400-88961400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:88959800-88961200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr3:88959800-88962600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:88960000-88963200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:88960000-88963600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr3:88960400-88962400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr3:88960400-88962600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr3:88960400-88963000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr3:88960600-88961600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr3:88960600-88962200	Enhancers	Brain Substantia Nigra	brain
37	chr3:88960600-88962400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr3:88960600-88962400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr3:88960600-88962600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr3:88961000-88962400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr3:88961200-88961600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr3:88961200-88962000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr3:88961200-88962000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:88961200-88962000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr3:88961200-88962400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr3:88961200-88962400	Enhancers	Brain Anterior Caudate	brain
47	chr3:88961200-88962400	Enhancers	Brain Cingulate Gyrus	brain
48	chr3:88961200-88962400	Enhancers	Brain Germinal Matrix	brain
49	chr3:88961200-88962600	Enhancers	Brain Angular Gyrus	brain
50	chr3:88961200-88962600	Enhancers	Brain Hippocampus Middle	brain

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