Variant report

Variant	nsv833792
Chromosome Location	chr2:36370408-36549413
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	ARID3A	chr2:36392370-36392619	HepG2	liver:	n/a	n/a
2	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
3	ATF2	chr2:36473354-36473889	GM12878	blood:	n/a	n/a
4	ATF2	chr2:36473245-36473881	GM12878	blood:	n/a	n/a
5	ATF2	chr2:36497853-36498342	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:36417402-36417520	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:36545626-36545719	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:36474136-36474343	GM12878	blood:	n/a	chr2:36474255-36474266
9	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
10	BATF	chr2:36473528-36473788	GM12878	blood:	n/a	n/a
11	BATF	chr2:36467483-36467862	GM12878	blood:	n/a	n/a
12	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:36473409-36473790	GM12878	blood:	n/a	chr2:36473585-36473594
14	BCL11A	chr2:36497933-36498242	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
16	BCL11A	chr2:36506762-36507002	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr2:36473447-36473808	GM12878	blood:	n/a	chr2:36473585-36473594
18	BCLAF1	chr2:36473380-36473879	GM12878	blood:	n/a	chr2:36473585-36473594
19	BCLAF1	chr2:36467548-36468268	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:36411001-36411307	HepG2	liver:	n/a	n/a
21	BRCA1	chr2:36546010-36546093	HepG2	liver:	n/a	n/a
22	BRCA1	chr2:36473771-36473792	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:36420172-36420519	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
24	CEBPB	chr2:36526504-36526612	IMR90	lung:	n/a	chr2:36526529-36526540
25	CEBPB	chr2:36374813-36375491	IMR90	lung:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
26	CEBPB	chr2:36395338-36395598	Hela-S3	cervix:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
27	CEBPB	chr2:36379312-36379579	HepG2	liver:	n/a	chr2:36379457-36379468
28	CEBPB	chr2:36449665-36449982	A549	lung:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822
29	CEBPB	chr2:36374848-36374960	HepG2	liver:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
30	CEBPB	chr2:36549402-36549551	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:36506728-36507022	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:36395475-36395510	IMR90	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
33	CEBPB	chr2:36434672-36434980	HepG2	liver:	n/a	chr2:36434830-36434841
34	CEBPB	chr2:36514592-36514954	Hela-S3	cervix:	n/a	chr2:36514780-36514791
35	CEBPB	chr2:36526442-36526614	HepG2	liver:	n/a	chr2:36526529-36526540
36	CEBPB	chr2:36514601-36514964	HepG2	liver:	n/a	chr2:36514780-36514791
37	CEBPB	chr2:36434705-36434959	A549	lung:	n/a	chr2:36434830-36434841
38	CEBPB	chr2:36449657-36449993	HepG2	liver:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822
39	CEBPB	chr2:36380814-36381038	IMR90	lung:	n/a	chr2:36380974-36380985
40	CEBPB	chr2:36449665-36449997	IMR90	lung:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822
41	CEBPB	chr2:36395379-36395613	A549	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
42	CEBPB	chr2:36419090-36419285	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:36497871-36498193	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr2:36375217-36375486	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:36437530-36437813	HepG2	liver:	n/a	chr2:36437627-36437638
46	CEBPB	chr2:36498605-36498713	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr2:36514610-36514947	A549	lung:	n/a	chr2:36514780-36514791
48	CEBPB	chr2:36514534-36514969	IMR90	lung:	n/a	chr2:36514780-36514791
49	CEBPB	chr2:36395324-36395659	HepG2	liver:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
50	CEBPB	chr2:36437519-36437741	A549	lung:	n/a	chr2:36437627-36437638

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36467699-36467749	HepG2	liver:	n/a
2	chr2:36467699-36467749	HepG2	liver:	n/a
3	chr2:36441749-36441799	NT2-D1	testis:	n/a
4	chr2:36467699-36467749	HNPCEpiC	eye:	n/a
5	chr2:36406592-36406642	HAEpiC	amniotic membrane:	n/a
6	chr2:36441749-36441799	SK-N-SH	brain:	n/a
7	chr2:36467699-36467749	HEEpiC	esophagus:	n/a
8	chr2:36406592-36406642	AG09309	skin:	n/a
9	chr2:36406592-36406642	NHDF-neo	bronchial:	n/a
10	chr2:36406592-36406642	NH-A	brain:	n/a
11	chr2:36406592-36406642	SK-N-SH	brain:	n/a
12	chr2:36441749-36441799	HRCEpiC	kidney:	n/a
13	chr2:36406592-36406642	T-47D	breast:	n/a
14	chr2:36441749-36441799	Jurkat	blood:	n/a
15	chr2:36467699-36467749	HRCEpiC	kidney:	n/a
16	chr2:36441749-36441799	AG04450	lung:	fetal
17	chr2:36467699-36467749	PrEC	prostate:	n/a
18	chr2:36441749-36441799	K562	blood:	n/a
19	chr2:36406592-36406642	Caco-2	colon:	n/a
20	chr2:36467699-36467749	BE2_C	brain:	n/a
21	chr2:36441749-36441799	SK-N-SH_RA	brain:	n/a
22	chr2:36467699-36467749	AG09309	skin:	n/a
23	chr2:36406592-36406642	HIPEpiC	eye:	n/a
24	chr2:36406592-36406642	AG10803	skin:	n/a
25	chr2:36467699-36467749	AG04450	lung:	fetal
26	chr2:36441749-36441799	AG10803	skin:	n/a
27	chr2:36441749-36441799	GM06990	blood:	n/a
28	chr2:36406592-36406642	HCF	heart:	n/a
29	chr2:36467699-36467749	AG10803	skin:	n/a
30	chr2:36406592-36406642	HRCEpiC	kidney:	n/a
31	chr2:36441749-36441799	T-47D	breast:	n/a
32	chr2:36441749-36441799	HNPCEpiC	eye:	n/a
33	chr2:36467699-36467749	RPTEC	kidney:	n/a
34	chr2:36441749-36441799	HAEpiC	amniotic membrane:	n/a
35	chr2:36406592-36406642	NB4	blood:	n/a
36	chr2:36441749-36441799	AG09319	gingival:	n/a
37	chr2:36441749-36441799	HCM	heart:	n/a
38	chr2:36406592-36406642	HCPEpiC	choroid plexus:	n/a
39	chr2:36406592-36406642	PrEC	prostate:	n/a
40	chr2:36441749-36441799	NHBE	bronchial:	n/a
41	chr2:36441749-36441799	LNCaP	prostate:	n/a
42	chr2:36441749-36441799	HCF	heart:	n/a
43	chr2:36441749-36441799	RPTEC	kidney:	n/a
44	chr2:36467699-36467749	GM12892	blood:	n/a
45	chr2:36406592-36406642	ProgFib	skin:	n/a
46	chr2:36441749-36441799	SKMC	muscle:	n/a
47	chr2:36467699-36467749	Jurkat	blood:	n/a
48	chr2:36406592-36406642	AoSMC	blood vessel:	n/a
49	chr2:36406592-36406642	HEEpiC	esophagus:	n/a
50	chr2:36406592-36406642	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
2	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
3	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
4	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
5	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
6	chr2:36463029..36465414-chr20:47894852..47896594,2	K562	blood:
7	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
8	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-5	chr2:36526531-36526973	NONHSAT070076

Variant related genes	Relation type
ENSG00000233752	TF binding region
ENSG00000233752	CpG island
ENSG00000177410	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000124201	chromatin interactions

Extended variants
information (count: 5615 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:5615 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140941328	chr2:36373017-36373018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142816536	chr2:36373029-36373030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186777339	chr2:36373031-36373032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538722636	chr2:36373037-36373038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556914747	chr2:36373054-36373055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575103106	chr2:36373055-36373056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535995352	chr2:36373112-36373113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554465880	chr2:36373135-36373136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192411863	chr2:36373159-36373160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1167447	chr2:36373160-36373161	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs116789520	chr2:36373179-36373180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577315023	chr2:36373185-36373186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368836259	chr2:36373186-36373187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185575395	chr2:36373244-36373245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190462522	chr2:36373267-36373268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78588504	chr2:36373301-36373302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181641287	chr2:36373334-36373335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527977174	chr2:36373344-36373345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546323805	chr2:36373349-36373350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571211468	chr2:36373350-36373351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531968032	chr2:36373367-36373368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1167448	chr2:36373424-36373425	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs371639994	chr2:36373428-36373429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541408988	chr2:36373433-36373434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373112532	chr2:36373519-36373520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536056981	chr2:36373525-36373526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185192559	chr2:36373626-36373627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374982566	chr2:36373644-36373645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs367961499	chr2:36373647-36373648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201240387	chr2:36373648-36373649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566455970	chr2:36373669-36373670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77723519	chr2:36373685-36373686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188671951	chr2:36373702-36373703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs62134064	chr2:36373724-36373725	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs577178418	chr2:36373729-36373730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553405936	chr2:36373802-36373803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375140526	chr2:36373803-36373804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181381441	chr2:36373849-36373850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556642108	chr2:36373854-36373855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542478858	chr2:36373914-36373915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185218463	chr2:36373920-36373921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113453192	chr2:36373921-36373922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546483568	chr2:36373922-36373923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13000033	chr2:36373966-36373967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542955669	chr2:36373970-36373971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1167449	chr2:36373980-36373981	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs532154879	chr2:36373992-36373993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189727902	chr2:36374007-36374008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377211186	chr2:36374025-36374026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568435865	chr2:36374051-36374052	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36373000-36373200	Enhancers	Pancreas	Pancrea
2	chr2:36373000-36374000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr2:36373200-36375200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr2:36373800-36374600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr2:36374000-36374400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr2:36374200-36374600	Enhancers	GM12878-XiMat	blood
7	chr2:36374600-36375000	Enhancers	Adipose Nuclei	Adipose
8	chr2:36374600-36375000	Flanking Active TSS	GM12878-XiMat	blood
9	chr2:36375000-36375400	Enhancers	GM12878-XiMat	blood
10	chr2:36376400-36376800	Active TSS	Brain Inferior Temporal Lobe	brain
11	chr2:36376400-36377000	Enhancers	Brain Substantia Nigra	brain
12	chr2:36376400-36377400	Enhancers	Brain Germinal Matrix	brain
13	chr2:36376600-36376800	Active TSS	Brain Hippocampus Middle	brain
14	chr2:36376800-36377400	Flanking Active TSS	Brain Hippocampus Middle	brain
15	chr2:36377000-36377200	Active TSS	Brain Substantia Nigra	brain
16	chr2:36377000-36377400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr2:36377000-36377400	Enhancers	HSMMtube	muscle
18	chr2:36377200-36377400	Flanking Active TSS	Brain Substantia Nigra	brain
19	chr2:36377200-36378000	Enhancers	Fetal Brain Female	brain
20	chr2:36377400-36378200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:36378200-36379000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:36378600-36379000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr2:36387800-36388400	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr2:36388400-36390400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr2:36390400-36391400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:36390400-36391400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:36391000-36394400	Enhancers	Liver	Liver
28	chr2:36391200-36391400	Bivalent Enhancer	A549	lung
29	chr2:36391400-36392400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr2:36391800-36393200	Enhancers	HepG2	liver
31	chr2:36392000-36392800	Enhancers	Fetal Intestine Small	intestine
32	chr2:36392400-36394000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr2:36393800-36394000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:36394000-36395200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr2:36395200-36395600	Enhancers	HMEC	breast
36	chr2:36395200-36403400	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr2:36395600-36400200	Weak transcription	HMEC	breast
38	chr2:36397800-36398400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:36397800-36401400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:36398000-36398200	Enhancers	Fetal Kidney	kidney
41	chr2:36398000-36398200	Enhancers	HSMMtube	muscle
42	chr2:36398400-36399400	Weak transcription	Fetal Kidney	kidney
43	chr2:36399200-36400400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:36399400-36401000	Enhancers	Fetal Kidney	kidney
45	chr2:36399400-36401400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:36400000-36400200	Enhancers	Esophagus	oesophagus
47	chr2:36400200-36400800	Weak transcription	Esophagus	oesophagus
48	chr2:36400200-36402000	Enhancers	HMEC	breast
49	chr2:36400400-36401400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:36400600-36401600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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