Variant report

Variant	nsv876285
Chromosome Location	chr3:182674-258123
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:1162)
Chromatin interactive
region (count:4)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:254017-254518	GM12878	blood:	n/a	n/a
2	ATF2	chr3:254098-254530	GM12878	blood:	n/a	n/a
3	BACH1	chr3:238826-240389	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:238302-238499	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:254085-254416	GM12878	blood:	n/a	n/a
6	CCNT2	chr3:238979-239034	K562	blood:	n/a	n/a
7	CCNT2	chr3:210502-210583	K562	blood:	n/a	n/a
8	CEBPB	chr3:216138-216415	Hela-S3	cervix:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
9	CEBPB	chr3:242454-242771	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr3:216151-216444	HepG2	liver:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
11	CEBPB	chr3:242488-242808	A549	lung:	n/a	n/a
12	CEBPB	chr3:215340-215517	A549	lung:	n/a	chr3:215398-215409 chr3:215397-215410
13	CEBPB	chr3:243976-244300	IMR90	lung:	n/a	chr3:244109-244120
14	CEBPB	chr3:219216-219513	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:244050-244226	H1-hESC	embryonic stem cell:	n/a	chr3:244109-244120
16	CEBPB	chr3:242500-242742	K562	blood:	n/a	n/a
17	CEBPB	chr3:242447-242817	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:219203-219482	A549	lung:	n/a	n/a
19	CEBPB	chr3:243974-244307	A549	lung:	n/a	chr3:244109-244120
20	CEBPB	chr3:215306-215533	K562	blood:	n/a	chr3:215398-215409 chr3:215397-215410
21	CEBPB	chr3:211035-211283	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:216135-216492	A549	lung:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
23	CEBPB	chr3:215234-215549	HepG2	liver:	n/a	chr3:215398-215409 chr3:215397-215410
24	CEBPB	chr3:242440-242811	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:243949-244303	HepG2	liver:	n/a	chr3:244109-244120
26	CHD1	chr3:239582-239589	GM12878	blood:	n/a	n/a
27	CHD1	chr3:195466-195490	GM12878	blood:	n/a	n/a
28	CHD1	chr3:239219-239240	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr3:238324-238476	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr3:238225-238590	GM12878	blood:	n/a	n/a
31	CREB1	chr3:254049-254528	GM12878	blood:	n/a	n/a
32	CTBP2	chr3:238125-240202	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr3:249780-249930	GM12870	blood:	n/a	n/a
34	CTCF	chr3:237340-237490	BE2_C	brain:	n/a	n/a
35	CTCF	chr3:237460-237610	HRE	kidney:	n/a	n/a
36	CTCF	chr3:249780-249930	HMF	breast:	n/a	n/a
37	CTCF	chr3:249780-249930	SAEC	small airway:	n/a	n/a
38	CTCF	chr3:197900-198050	NHEK	skin:	n/a	n/a
39	CTCF	chr3:197800-197950	HAc	cerebellar:	n/a	n/a
40	CTCF	chr3:207280-207430	GM12872	blood:	n/a	n/a
41	CTCF	chr3:237440-237590	GM12873	blood:	n/a	n/a
42	CTCF	chr3:249780-249930	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr3:239640-239790	GM12872	blood:	n/a	n/a
44	CTCF	chr3:249700-249850	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr3:249740-249890	NHEK	skin:	n/a	n/a
46	CTCF	chr3:249760-249910	GM12865	blood:	n/a	n/a
47	CTCF	chr3:209455-209509	GM20000	blood:	n/a	n/a
48	CTCF	chr3:239600-239750	GM12869	blood:	n/a	n/a
49	CTCF	chr3:249740-249890	GM12874	blood:	n/a	n/a
50	CTCF	chr3:237400-237550	HEK293	kidney:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:236078-236128	RPTEC	kidney:	n/a
2	chr3:239229-239279	GM19239	blood:	n/a
3	chr3:238318-238368	SKMC	muscle:	n/a
4	chr3:236078-236128	RPTEC	kidney:	n/a
5	chr3:239229-239279	GM19239	blood:	n/a
6	chr3:238318-238368	SKMC	muscle:	n/a
7	chr3:238318-238368	GM12878	blood:	n/a
8	chr3:239733-239783	NHBE	bronchial:	n/a
9	chr3:239229-239279	AoSMC	blood vessel:	n/a
10	chr3:238318-238368	HL-60	blood:	n/a
11	chr3:243996-244046	Hela-S3	cervix:	n/a
12	chr3:238611-238661	ECC-1	luminal epithelium:	n/a
13	chr3:238048-238098	SK-N-SH	brain:	n/a
14	chr3:238618-238668	NHBE	bronchial:	n/a
15	chr3:239665-239715	HAEpiC	amniotic membrane:	n/a
16	chr3:243996-244046	GM06990	blood:	n/a
17	chr3:238392-238442	SAEC	small airway:	n/a
18	chr3:240139-240189	RPTEC	kidney:	n/a
19	chr3:239229-239279	AG09309	skin:	n/a
20	chr3:239665-239715	HPAEpiC	pulmonary alveolar:	n/a
21	chr3:236078-236128	Hepatocyte	liver:	n/a
22	chr3:238611-238661	HEK293	kidney:	embryo
23	chr3:239188-239238	U87	brain:	n/a
24	chr3:239188-239238	A549	lung:	n/a
25	chr3:239207-239257	HCM	heart:	n/a
26	chr3:239188-239238	HIPEpiC	eye:	n/a
27	chr3:239188-239238	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:238392-238442	ProgFib	skin:	n/a
29	chr3:238161-238211	RPTEC	kidney:	n/a
30	chr3:240139-240189	ProgFib	skin:	n/a
31	chr3:240139-240189	HRCEpiC	kidney:	n/a
32	chr3:239207-239257	NB4	blood:	n/a
33	chr3:238161-238211	HEK293	kidney:	embryo
34	chr3:239506-239556	HL-60	blood:	n/a
35	chr3:236078-236128	HNPCEpiC	eye:	n/a
36	chr3:238496-238546	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:239665-239715	NT2-D1	testis:	n/a
38	chr3:239665-239715	HRE	kidney:	n/a
39	chr3:243996-244046	PANC-1	pancreas:	n/a
40	chr3:238048-238098	CMK	blood:	n/a
41	chr3:238611-238661	RPTEC	kidney:	n/a
42	chr3:241182-241232	Hepatocyte	liver:	n/a
43	chr3:238161-238211	GM06990	blood:	n/a
44	chr3:239229-239279	MCF10A-Er-Src	breast:	n/a
45	chr3:239229-239279	GM12892	blood:	n/a
46	chr3:243996-244046	AG04450	lung:	fetal
47	chr3:239229-239279	HL-60	blood:	n/a
48	chr3:238611-238661	PFSK-1	brain:	n/a
49	chr3:238615-238665	HCM	heart:	n/a
50	chr3:238615-238665	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:217250..219144-chr3:222760..225297,2	MCF-7	breast:
2	chr3:188824..190368-chr3:386265..388997,2	MCF-7	breast:
3	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
4	chr3:217250..219144-chr3:222760..225297,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL5RA-6	chr3:237679-237723	NONHSAT087559
2	lnc-CNTN6-7	chr3:239697-239775	NONHSAT087562
3	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
4	lnc-IL5RA-6	chr3:238650-239024	ENSG00000224318.1
5	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
6	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
7	lnc-CNTN6-7	chr3:254887-255362	NONHSAT087562
8	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
9	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
10	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
11	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
12	lnc-IL5RA-6	chr3:237540-237597	NONHSAT087559
13	lnc-IL5RA-6	chr3:238290-238542	ENSG00000224318.1
14	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
15	lnc-CNTN6-7	chr3:239326-239775	NONHSAT087561
16	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
17	lnc-IL5RA-6	chr3:238290-238385	ENSG00000224318.1
18	lnc-CNTN6-7	chr3:238454-238746	NONHSAT087560
19	lnc-IL5RA-6	chr3:238650-238882	ENSG00000224318.1
20	lnc-IL5RA-6	chr3:238139-238386	NONHSAT087559

No data

Variant related genes	Relation type
CHL1	TF binding region
CHL1-AS2	TF binding region
CHL1	CpG island
CHL1-AS2	CpG island

Extended variants
information (count: 2158 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2158 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1400179	chr3:182674-182675	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571592043	chr3:182675-182676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538979759	chr3:182679-182680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375675423	chr3:182686-182687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377725119	chr3:182741-182742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139800691	chr3:182770-182771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570010337	chr3:182771-182772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369645976	chr3:182778-182779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536836652	chr3:182806-182807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149763295	chr3:182807-182808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537352041	chr3:182811-182812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180835133	chr3:182820-182821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537095777	chr3:182821-182822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185187380	chr3:182833-182834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35716412	chr3:182843-182844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111246467	chr3:182847-182848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576735993	chr3:182864-182865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561491227	chr3:182902-182903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558489214	chr3:182912-182913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11717011	chr3:182913-182914	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs553208609	chr3:182920-182921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574336388	chr3:182943-182944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190045113	chr3:182947-182948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563097606	chr3:182978-182979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531716375	chr3:182979-182980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6797567	chr3:183023-183024	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs34807518	chr3:183057-183058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183337561	chr3:183101-183102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146798330	chr3:183118-183119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547823266	chr3:183121-183122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139961551	chr3:183130-183131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574874176	chr3:183131-183132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530376416	chr3:183155-183156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548803025	chr3:183168-183169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116431057	chr3:189814-189815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184536868	chr3:189819-189820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553177931	chr3:189863-189864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544995224	chr3:189914-189915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561620734	chr3:189947-189948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370956817	chr3:189955-189956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573643294	chr3:189994-189995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543866306	chr3:189995-189996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562473133	chr3:190004-190005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568215582	chr3:190028-190029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115254867	chr3:190030-190031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115817282	chr3:190045-190046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547154906	chr3:190053-190054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568465550	chr3:190062-190063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535917310	chr3:190067-190068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550714074	chr3:190069-190070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Thoracic aortic aneurysm	21092924	CNVD

Chromatin state (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:181600-182800	Enhancers	Colon Smooth Muscle	Colon
2	chr3:182000-182800	Enhancers	Fetal Brain Female	brain
3	chr3:182000-183200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr3:182200-182800	Enhancers	Rectal Smooth Muscle	rectum
5	chr3:182600-183000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:182600-183000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:182600-183000	Enhancers	Ovary	ovary
8	chr3:189800-190200	Enhancers	Brain Germinal Matrix	brain
9	chr3:189800-193200	Weak transcription	Ovary	ovary
10	chr3:193200-193600	Enhancers	Primary B cells from peripheral blood	blood
11	chr3:193200-193600	Enhancers	Ovary	ovary
12	chr3:197000-198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr3:197600-198200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:201000-203000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr3:201200-201600	Enhancers	Primary hematopoietic stem cells	blood
16	chr3:201400-202800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr3:202600-202800	Enhancers	Primary hematopoietic stem cells	blood
18	chr3:204400-204600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr3:205600-206000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:205600-206800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:205800-206000	Enhancers	Brain Substantia Nigra	brain
22	chr3:206000-206200	Enhancers	Fetal Brain Female	brain
23	chr3:206000-207200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:206000-207600	Weak transcription	Brain Substantia Nigra	brain
25	chr3:206000-209000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr3:206200-207200	Weak transcription	Fetal Brain Female	brain
27	chr3:206400-209000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:206400-209000	Enhancers	Brain Germinal Matrix	brain
29	chr3:206600-209200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:206800-207200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr3:207200-207800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:207200-207800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:207200-208400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:207200-209000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:207200-209000	Enhancers	Fetal Brain Female	brain
36	chr3:207400-207800	Enhancers	Brain Angular Gyrus	brain
37	chr3:207400-208000	Enhancers	Brain Cingulate Gyrus	brain
38	chr3:207600-207800	Enhancers	Brain Hippocampus Middle	brain
39	chr3:207600-208000	Enhancers	Brain Anterior Caudate	brain
40	chr3:207600-208000	Enhancers	Brain Substantia Nigra	brain
41	chr3:207800-209000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:207800-215200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:209000-209200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:215200-215400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:215400-215600	Enhancers	Adipose Nuclei	Adipose
46	chr3:215400-215600	Enhancers	GM12878-XiMat	blood
47	chr3:215400-215800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr3:215400-215800	Active TSS	Brain Anterior Caudate	brain
49	chr3:215400-216000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:215400-216000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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