Variant report

Variant	nsv998827
Chromosome Location	chr3:212710-274182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:1223)
Chromatin interactive
region (count:2)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:278 , 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	chr3:254098-254530	GM12878	blood:	n/a	n/a
2	ATF2	chr3:254017-254518	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	BACH1	chr3:271174-271333	K562	blood:	n/a	n/a
6	BATF	chr3:259675-259847	GM12878	blood:	n/a	n/a
7	BATF	chr3:254085-254416	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:260263-260618	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:260829-261058	GM12878	blood:	n/a	n/a
10	CCNT2	chr3:238979-239034	K562	blood:	n/a	n/a
11	CEBPB	chr3:215306-215533	K562	blood:	n/a	chr3:215398-215409 chr3:215397-215410
12	CEBPB	chr3:219203-219482	A549	lung:	n/a	n/a
13	CEBPB	chr3:243974-244307	A549	lung:	n/a	chr3:244109-244120
14	CEBPB	chr3:242447-242817	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:215340-215517	A549	lung:	n/a	chr3:215398-215409 chr3:215397-215410
16	CEBPB	chr3:216135-216492	A549	lung:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
17	CEBPB	chr3:271018-271333	H1-hESC	embryonic stem cell:	n/a	chr3:271305-271317
18	CEBPB	chr3:243949-244303	HepG2	liver:	n/a	chr3:244109-244120
19	CEBPB	chr3:244050-244226	H1-hESC	embryonic stem cell:	n/a	chr3:244109-244120
20	CEBPB	chr3:215234-215549	HepG2	liver:	n/a	chr3:215398-215409 chr3:215397-215410
21	CEBPB	chr3:216138-216415	Hela-S3	cervix:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
22	CEBPB	chr3:243976-244300	IMR90	lung:	n/a	chr3:244109-244120
23	CEBPB	chr3:242488-242808	A549	lung:	n/a	n/a
24	CEBPB	chr3:242440-242811	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:216151-216444	HepG2	liver:	n/a	chr3:216322-216333 chr3:216301-216314 chr3:216321-216334 chr3:216302-216313
26	CEBPB	chr3:242454-242771	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:242500-242742	K562	blood:	n/a	n/a
28	CEBPB	chr3:219216-219513	HepG2	liver:	n/a	n/a
29	CHD1	chr3:239219-239240	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr3:239582-239589	GM12878	blood:	n/a	n/a
31	CHD1	chr3:238324-238476	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr3:238225-238590	GM12878	blood:	n/a	n/a
33	CREB1	chr3:254049-254528	GM12878	blood:	n/a	n/a
34	CTBP2	chr3:238125-240202	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr3:249740-249890	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr3:249780-249930	NB4	blood:	n/a	n/a
37	CTCF	chr3:249660-249810	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr3:239600-239750	GM12869	blood:	n/a	n/a
39	CTCF	chr3:249720-249870	GM12864	blood:	n/a	n/a
40	CTCF	chr3:212669-212747	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr3:249780-249930	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:249700-249850	GM12873	blood:	n/a	n/a
43	CTCF	chr3:249740-249890	GM12878	blood:	n/a	n/a
44	CTCF	chr3:249720-249870	HRE	kidney:	n/a	n/a
45	CTCF	chr3:249780-249930	SAEC	small airway:	n/a	n/a
46	CTCF	chr3:237402-237596	GM12878	blood:	n/a	n/a
47	CTCF	chr3:249820-249970	GM12867	blood:	n/a	n/a
48	CTCF	chr3:249740-249890	GM12875	blood:	n/a	n/a
49	CTCF	chr3:237440-237590	GM12873	blood:	n/a	n/a
50	CTCF	chr3:249480-249630	HEEpiC	esophagus:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:238931-238981	ProgFib	skin:	n/a
2	chr3:238931-238981	HRE	kidney:	n/a
3	chr3:238318-238368	HRE	kidney:	n/a
4	chr3:238931-238981	ProgFib	skin:	n/a
5	chr3:238931-238981	HRE	kidney:	n/a
6	chr3:238318-238368	HRE	kidney:	n/a
7	chr3:239207-239257	HUVEC	blood vessel:	n/a
8	chr3:238048-238098	GM12892	blood:	n/a
9	chr3:238496-238546	AG09309	skin:	n/a
10	chr3:238318-238368	GM12878	blood:	n/a
11	chr3:241182-241232	PrEC	prostate:	n/a
12	chr3:241182-241232	GM12878	blood:	n/a
13	chr3:243996-244046	SK-N-MC	brain:	n/a
14	chr3:241182-241232	NHDF-neo	bronchial:	n/a
15	chr3:238931-238981	GM12891	blood:	n/a
16	chr3:239188-239238	GM19239	blood:	n/a
17	chr3:239207-239257	PrEC	prostate:	n/a
18	chr3:240139-240189	IMR90	lung:	fetal
19	chr3:238618-238668	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:238161-238211	AG09319	gingival:	n/a
21	chr3:238618-238668	GM06990	blood:	n/a
22	chr3:238496-238546	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:239207-239257	HCT-116	colon:	n/a
24	chr3:238615-238665	MCF10A-Er-Src	breast:	n/a
25	chr3:238618-238668	AG04450	lung:	fetal
26	chr3:239733-239783	NHBE	bronchial:	n/a
27	chr3:239665-239715	SK-N-SH	brain:	n/a
28	chr3:238318-238368	AG10803	skin:	n/a
29	chr3:236078-236128	NB4	blood:	n/a
30	chr3:238611-238661	MCF-7	breast:	n/a
31	chr3:239207-239257	T-47D	breast:	n/a
32	chr3:239207-239257	GM19239	blood:	n/a
33	chr3:238496-238546	HCT-116	colon:	n/a
34	chr3:238496-238546	SK-N-SH	brain:	n/a
35	chr3:243996-244046	HL-60	blood:	n/a
36	chr3:238048-238098	AG09319	gingival:	n/a
37	chr3:238615-238665	SK-N-SH	brain:	n/a
38	chr3:238392-238442	SAEC	small airway:	n/a
39	chr3:240139-240189	MCF-7	breast:	n/a
40	chr3:238392-238442	SK-N-SH_RA	brain:	n/a
41	chr3:239665-239715	HCF	heart:	n/a
42	chr3:243996-244046	GM12892	blood:	n/a
43	chr3:243996-244046	HCF	heart:	n/a
44	chr3:239207-239257	NHBE	bronchial:	n/a
45	chr3:239188-239238	HUVEC	blood vessel:	n/a
46	chr3:239665-239715	SKMC	muscle:	n/a
47	chr3:239229-239279	HEEpiC	esophagus:	n/a
48	chr3:241182-241232	BJ	skin:	n/a
49	chr3:243996-244046	NHBE	bronchial:	n/a
50	chr3:241182-241232	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:217250..219144-chr3:222760..225297,2	MCF-7	breast:
2	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	chr3:237441-237597	ENSG00000224318.1
2	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
3	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
4	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
5	lnc-IL5RA-6	chr3:238290-238542	ENSG00000224318.1
6	lnc-CNTN6-7	chr3:254887-255362	NONHSAT087562
7	lnc-CNTN6-7	chr3:239697-239775	NONHSAT087562
8	lnc-IL5RA-6	chr3:238650-239024	ENSG00000224318.1
9	lnc-IL5RA-6	chr3:237540-237597	NONHSAT087559
10	lnc-CNTN6-7	chr3:239326-239775	NONHSAT087561
11	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
12	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
13	lnc-IL5RA-6	chr3:238650-238882	ENSG00000224318.1
14	lnc-IL5RA-6	chr3:238290-238385	ENSG00000224318.1
15	lnc-IL5RA-6	chr3:237679-237723	NONHSAT087559
16	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
17	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
18	lnc-CNTN6-7	chr3:238454-238746	NONHSAT087560
19	lnc-IL5RA-6	chr3:238139-238386	NONHSAT087559
20	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1

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: 2181 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2181 , 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	rs150769757	chr3:212731-212732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376667928	chr3:212738-212739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186599934	chr3:212742-212743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs28464768	chr3:212751-212752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189872759	chr3:212760-212761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139126915	chr3:212761-212762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542172340	chr3:212790-212791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149931389	chr3:212842-212843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555963584	chr3:212905-212906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182450830	chr3:212911-212912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369121939	chr3:212972-212973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17041615	chr3:212991-212992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs570702971	chr3:213006-213007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538473584	chr3:213030-213031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188247610	chr3:213034-213035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76923041	chr3:213035-213036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573544477	chr3:213060-213061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192758750	chr3:213062-213063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568518975	chr3:213085-213086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199961215	chr3:213093-213094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568121161	chr3:213096-213097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185217094	chr3:213108-213109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556983181	chr3:213111-213112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569205634	chr3:213125-213126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375447734	chr3:213128-213129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539732081	chr3:213171-213172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78360213	chr3:213190-213191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140414468	chr3:213202-213203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1124026	chr3:213222-213223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs553205521	chr3:213227-213228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545336596	chr3:213232-213233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112775874	chr3:213249-213250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1567789	chr3:213257-213258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs116145977	chr3:213259-213260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78913946	chr3:213292-213293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546098518	chr3:213299-213300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188468536	chr3:213301-213302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528702489	chr3:213363-213364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528766763	chr3:213371-213372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7613220	chr3:213398-213399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377497373	chr3:213401-213402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550646289	chr3:213413-213414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34202206	chr3:213441-213442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568876454	chr3:213470-213471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562887483	chr3:213476-213477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192311959	chr3:213501-213502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141855086	chr3:213508-213509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184741315	chr3:213515-213516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189494478	chr3:213525-213526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1151145	chr3:213597-213598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:207800-215200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr3:215200-215400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:215400-215600	Enhancers	Adipose Nuclei	Adipose
4	chr3:215400-215600	Enhancers	GM12878-XiMat	blood
5	chr3:215400-215800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr3:215400-215800	Active TSS	Brain Anterior Caudate	brain
7	chr3:215400-216000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:215400-216000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr3:215400-216200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:215600-215800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr3:215600-215800	Flanking Active TSS	Liver	Liver
12	chr3:215600-216000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr3:215600-216000	Flanking Active TSS	Adipose Nuclei	Adipose
14	chr3:215600-216000	Flanking Active TSS	GM12878-XiMat	blood
15	chr3:215600-216200	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr3:215800-216000	Active TSS	Liver	Liver
17	chr3:215800-216200	Enhancers	Primary B cells from peripheral blood	blood
18	chr3:215800-216200	Enhancers	Brain Anterior Caudate	brain
19	chr3:216000-216200	Enhancers	Adipose Nuclei	Adipose
20	chr3:216000-216400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:216200-217000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr3:225200-225600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:226600-227000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr3:233600-233800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr3:233600-234400	Enhancers	Primary B cells from peripheral blood	blood
26	chr3:233800-235000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr3:234200-234800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
28	chr3:234600-234800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
29	chr3:235000-235200	Enhancers	Fetal Brain Female	brain
30	chr3:235000-236000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr3:235200-236000	Weak transcription	Fetal Brain Female	brain
32	chr3:235400-236600	Enhancers	Fetal Brain Male	brain
33	chr3:235800-236000	Enhancers	Adipose Nuclei	Adipose
34	chr3:235800-236400	Enhancers	Spleen	Spleen
35	chr3:235800-237000	Enhancers	Ovary	ovary
36	chr3:236000-236200	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr3:236000-236400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:236000-236600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr3:236000-236800	Enhancers	Fetal Brain Female	brain
40	chr3:236200-236400	Enhancers	Brain Cingulate Gyrus	brain
41	chr3:236200-236400	Enhancers	Brain Substantia Nigra	brain
42	chr3:236200-237800	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr3:236400-237000	Enhancers	Brain Germinal Matrix	brain
44	chr3:236400-237400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:236400-238200	Weak transcription	Spleen	Spleen
46	chr3:236600-237200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:236600-237200	Flanking Active TSS	Fetal Brain Male	brain
48	chr3:236800-238000	Active TSS	Fetal Brain Female	brain
49	chr3:237000-237200	Active TSS	Brain Germinal Matrix	brain
50	chr3:237000-237800	Enhancers	Cortex derived primary cultured neurospheres	brain

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