Variant report

Variant	nsv581466
Chromosome Location	chr2:36353996-36569014
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	chr2:36556942-36557316	HepG2	liver:	n/a	chr2:36557242-36557258
2	ARID3A	chr2:36566092-36566413	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:36392370-36392619	HepG2	liver:	n/a	n/a
4	ATF2	chr2:36497853-36498342	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:36473354-36473889	GM12878	blood:	n/a	n/a
6	ATF2	chr2:36473245-36473881	GM12878	blood:	n/a	n/a
7	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
8	BACH1	chr2:36545626-36545719	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:36417402-36417520	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
11	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
12	BATF	chr2:36474136-36474343	GM12878	blood:	n/a	chr2:36474255-36474266
13	BATF	chr2:36467483-36467862	GM12878	blood:	n/a	n/a
14	BATF	chr2:36473528-36473788	GM12878	blood:	n/a	n/a
15	BATF	chr2:36564561-36564770	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:36473409-36473790	GM12878	blood:	n/a	chr2:36473585-36473594
17	BCL11A	chr2:36497933-36498242	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
19	BCL11A	chr2:36506762-36507002	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL3	chr2:36565737-36566479	A549	lung:	n/a	n/a
21	BCL3	chr2:36473447-36473808	GM12878	blood:	n/a	chr2:36473585-36473594
22	BCLAF1	chr2:36473380-36473879	GM12878	blood:	n/a	chr2:36473585-36473594
23	BCLAF1	chr2:36467548-36468268	GM12878	blood:	n/a	n/a
24	BHLHE40	chr2:36411001-36411307	HepG2	liver:	n/a	n/a
25	BRCA1	chr2:36473771-36473792	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr2:36546010-36546093	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:36556102-36556393	A549	lung:	n/a	chr2:36556209-36556220
28	CEBPB	chr2:36395475-36395510	IMR90	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
29	CEBPB	chr2:36497871-36498193	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr2:36379331-36379617	A549	lung:	n/a	chr2:36379457-36379468
31	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
32	CEBPB	chr2:36567018-36567360	IMR90	lung:	n/a	n/a
33	CEBPB	chr2:36498605-36498713	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr2:36556126-36556356	HepG2	liver:	n/a	chr2:36556209-36556220
35	CEBPB	chr2:36526442-36526614	HepG2	liver:	n/a	chr2:36526529-36526540
36	CEBPB	chr2:36420172-36420519	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
37	CEBPB	chr2:36567022-36567363	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr2:36374793-36375473	Hela-S3	cervix:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
39	CEBPB	chr2:36565742-36566503	A549	lung:	n/a	n/a
40	CEBPB	chr2:36514655-36514886	H1-hESC	embryonic stem cell:	n/a	chr2:36514780-36514791
41	CEBPB	chr2:36374813-36375491	IMR90	lung:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
42	CEBPB	chr2:36434672-36434980	HepG2	liver:	n/a	chr2:36434830-36434841
43	CEBPB	chr2:36375197-36375400	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr2:36526504-36526612	IMR90	lung:	n/a	chr2:36526529-36526540
45	CEBPB	chr2:36514601-36514964	HepG2	liver:	n/a	chr2:36514780-36514791
46	CEBPB	chr2:36514592-36514954	Hela-S3	cervix:	n/a	chr2:36514780-36514791
47	CEBPB	chr2:36514610-36514947	A549	lung:	n/a	chr2:36514780-36514791
48	CEBPB	chr2:36354969-36355117	HepG2	liver:	n/a	chr2:36355034-36355045
49	CEBPB	chr2:36556053-36556379	IMR90	lung:	n/a	chr2:36556209-36556220
50	CEBPB	chr2:36449700-36449915	Hela-S3	cervix:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36406592-36406642	HIPEpiC	eye:	n/a
2	chr2:36406592-36406642	ECC-1	luminal epithelium:	n/a
3	chr2:36557755-36557805	IMR90	lung:	fetal
4	chr2:36406592-36406642	NH-A	brain:	n/a
5	chr2:36441749-36441799	Hela-S3	cervix:	n/a
6	chr2:36441749-36441799	HCPEpiC	choroid plexus:	n/a
7	chr2:36441749-36441799	HCM	heart:	n/a
8	chr2:36406592-36406642	PFSK-1	brain:	n/a
9	chr2:36441749-36441799	H1-hESC	embryonic stem cell:	embryo
10	chr2:36565096-36565146	AG10803	skin:	n/a
11	chr2:36406592-36406642	HRCEpiC	kidney:	n/a
12	chr2:36406592-36406642	NB4	blood:	n/a
13	chr2:36557755-36557805	SK-N-MC	brain:	n/a
14	chr2:36467699-36467749	MCF10A-Er-Src	breast:	n/a
15	chr2:36557755-36557805	ProgFib	skin:	n/a
16	chr2:36557755-36557805	AG09319	gingival:	n/a
17	chr2:36441749-36441799	NHDF-neo	bronchial:	n/a
18	chr2:36406592-36406642	AoSMC	blood vessel:	n/a
19	chr2:36565096-36565146	HCT-116	colon:	n/a
20	chr2:36406592-36406642	HL-60	blood:	n/a
21	chr2:36406592-36406642	PrEC	prostate:	n/a
22	chr2:36467699-36467749	PrEC	prostate:	n/a
23	chr2:36565096-36565146	CMK	blood:	n/a
24	chr2:36557755-36557805	GM06990	blood:	n/a
25	chr2:36467699-36467749	BJ	skin:	n/a
26	chr2:36441749-36441799	RPTEC	kidney:	n/a
27	chr2:36441749-36441799	IMR90	lung:	fetal
28	chr2:36565096-36565146	ovcar-3	ovarian:	n/a
29	chr2:36557755-36557805	RPTEC	kidney:	n/a
30	chr2:36406592-36406642	HCT-116	colon:	n/a
31	chr2:36406592-36406642	SKMC	muscle:	n/a
32	chr2:36441749-36441799	AG09309	skin:	n/a
33	chr2:36557755-36557805	HCT-116	colon:	n/a
34	chr2:36565096-36565146	GM12892	blood:	n/a
35	chr2:36441749-36441799	HUVEC	blood vessel:	n/a
36	chr2:36557755-36557805	AG04449	skin:	fetal
37	chr2:36441749-36441799	HRE	kidney:	n/a
38	chr2:36406592-36406642	HRPEpiC	eye:	n/a
39	chr2:36406592-36406642	MCF-7	breast:	n/a
40	chr2:36557755-36557805	ECC-1	luminal epithelium:	n/a
41	chr2:36441749-36441799	SKMC	muscle:	n/a
42	chr2:36565096-36565146	HAEpiC	amniotic membrane:	n/a
43	chr2:36557755-36557805	A549	lung:	n/a
44	chr2:36565096-36565146	GM06990	blood:	n/a
45	chr2:36557755-36557805	U87	brain:	n/a
46	chr2:36441749-36441799	NT2-D1	testis:	n/a
47	chr2:36441749-36441799	SK-N-SH_RA	brain:	n/a
48	chr2:36467699-36467749	ProgFib	skin:	n/a
49	chr2:36565096-36565146	GM12878	blood:	n/a
50	chr2:36467699-36467749	HIPEpiC	eye:	n/a

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	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
4	chr2:36463029..36465414-chr20:47894852..47896594,2	K562	blood:
5	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
6	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
7	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
8	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
9	chr2:36561664..36563772-chr2:36823426..36826394,2	MCF-7	breast:
10	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
ENSG00000124201	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000171055	chromatin interactions

Extended variants
information (count: 6889 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6889 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7596950	chr2:36353996-36353997	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189731281	chr2:36354021-36354022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74453804	chr2:36354022-36354023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553323935	chr2:36354023-36354024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549215490	chr2:36354039-36354040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555720749	chr2:36354127-36354128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573958830	chr2:36354183-36354184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78981686	chr2:36354190-36354191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs367545569	chr2:36354207-36354208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111803358	chr2:36354261-36354262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539036367	chr2:36354335-36354336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149471891	chr2:36354346-36354347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143091421	chr2:36354351-36354352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1022121	chr2:36354424-36354425	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs554774906	chr2:36354427-36354428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573076972	chr2:36354479-36354480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540616408	chr2:36354498-36354499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1858261	chr2:36354543-36354544	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148184966	chr2:36354599-36354600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545012007	chr2:36354616-36354617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116417437	chr2:36354619-36354620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1686103	chr2:36354621-36354622	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs542896388	chr2:36354639-36354640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372375477	chr2:36354640-36354641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182355542	chr2:36354641-36354642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575718608	chr2:36354654-36354655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113611359	chr2:36354678-36354679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75455638	chr2:36354679-36354680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs33946541	chr2:36354690-36354691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375169112	chr2:36354691-36354692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201901399	chr2:36354693-36354694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114295296	chr2:36354741-36354742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141167883	chr2:36354767-36354768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571523454	chr2:36354791-36354792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs532275057	chr2:36354792-36354793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200557832	chr2:36354798-36354799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550573537	chr2:36354799-36354800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568894505	chr2:36354800-36354801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558834232	chr2:36354818-36354819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114836569	chr2:36354830-36354831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554639783	chr2:36354883-36354884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147424816	chr2:36354893-36354894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534413483	chr2:36354895-36354896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113837513	chr2:36354897-36354898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577482441	chr2:36354919-36354920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116851113	chr2:36354963-36354964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557024416	chr2:36354971-36354972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11124496	chr2:36355005-36355006	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs542786287	chr2:36355024-36355025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139812652	chr2:36355052-36355053	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	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:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36350200-36354000	Weak transcription	Fetal Brain Male	brain
2	chr2:36353200-36354000	Enhancers	Brain Germinal Matrix	brain
3	chr2:36353600-36354400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:36354000-36354400	Weak transcription	Brain Germinal Matrix	brain
5	chr2:36354000-36355200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr2:36354000-36355400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:36354000-36356800	Enhancers	Fetal Brain Male	brain
8	chr2:36354400-36356200	Enhancers	Brain Germinal Matrix	brain
9	chr2:36354800-36355000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:36354800-36356200	Enhancers	Fetal Brain Female	brain
11	chr2:36355200-36357400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr2:36355400-36355800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr2:36355800-36356000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:36356000-36357600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:36356200-36357200	Weak transcription	Fetal Brain Female	brain
16	chr2:36356200-36357600	Weak transcription	Brain Germinal Matrix	brain
17	chr2:36357400-36357600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr2:36357400-36357600	Enhancers	Fetal Brain Female	brain
19	chr2:36357600-36357800	Enhancers	Brain Germinal Matrix	brain
20	chr2:36357600-36358000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:36357600-36360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:36358000-36360200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr2:36360200-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:36360800-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:36364400-36365200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr2:36364400-36365200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr2:36364600-36365000	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr2:36364600-36365200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr2:36364600-36365200	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr2:36364600-36365200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr2:36364600-36365200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr2:36364600-36365400	Enhancers	Primary T cells from cord blood	blood
33	chr2:36364600-36365400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr2:36364800-36365200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr2:36364800-36365200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr2:36364800-36365200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr2:36364800-36365200	Enhancers	Thymus	Thymus
38	chr2:36364800-36366000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr2:36365600-36365800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr2:36365600-36367200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:36365800-36366400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:36366200-36366800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:36366400-36367600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr2:36366600-36367000	Enhancers	Fetal Kidney	kidney
45	chr2:36367000-36367400	Active TSS	Fetal Kidney	kidney
46	chr2:36367200-36367600	Enhancers	Fetal Lung	lung
47	chr2:36367200-36367800	Enhancers	Fetal Stomach	stomach
48	chr2:36373000-36373200	Enhancers	Pancreas	Pancrea
49	chr2:36373000-36374000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr2:36373200-36375200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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