Variant report

Variant	nsv581465
Chromosome Location	chr2:36346005-36575659
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	ARID3A	chr2:36556942-36557316	HepG2	liver:	n/a	chr2:36557242-36557258
3	ARID3A	chr2:36566092-36566413	HepG2	liver:	n/a	n/a
4	ATF2	chr2:36473245-36473881	GM12878	blood:	n/a	n/a
5	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
6	ATF2	chr2:36473354-36473889	GM12878	blood:	n/a	n/a
7	ATF2	chr2:36497853-36498342	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:36417402-36417520	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:36545626-36545719	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:36564561-36564770	GM12878	blood:	n/a	n/a
11	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
12	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
13	BATF	chr2:36467483-36467862	GM12878	blood:	n/a	n/a
14	BATF	chr2:36473528-36473788	GM12878	blood:	n/a	n/a
15	BATF	chr2:36474136-36474343	GM12878	blood:	n/a	chr2:36474255-36474266
16	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
17	BCL11A	chr2:36473409-36473790	GM12878	blood:	n/a	chr2:36473585-36473594
18	BCL11A	chr2:36506762-36507002	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr2:36497933-36498242	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	chr2:36546010-36546093	HepG2	liver:	n/a	n/a
26	BRCA1	chr2:36473771-36473792	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:36434759-36434959	IMR90	lung:	n/a	chr2:36434830-36434841
28	CEBPB	chr2:36380814-36381038	IMR90	lung:	n/a	chr2:36380974-36380985
29	CEBPB	chr2:36420124-36420491	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
30	CEBPB	chr2:36514655-36514886	H1-hESC	embryonic stem cell:	n/a	chr2:36514780-36514791
31	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
32	CEBPB	chr2:36556053-36556379	IMR90	lung:	n/a	chr2:36556209-36556220
33	CEBPB	chr2:36514592-36514954	Hela-S3	cervix:	n/a	chr2:36514780-36514791
34	CEBPB	chr2:36514534-36514969	IMR90	lung:	n/a	chr2:36514780-36514791
35	CEBPB	chr2:36419090-36419285	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:36437530-36437813	HepG2	liver:	n/a	chr2:36437627-36437638
37	CEBPB	chr2:36556126-36556356	HepG2	liver:	n/a	chr2:36556209-36556220
38	CEBPB	chr2:36420172-36420519	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
39	CEBPB	chr2:36354969-36355117	HepG2	liver:	n/a	chr2:36355034-36355045
40	CEBPB	chr2:36506728-36507022	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr2:36395475-36395510	IMR90	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
42	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
43	CEBPB	chr2:36556102-36556393	A549	lung:	n/a	chr2:36556209-36556220
44	CEBPB	chr2:36498605-36498713	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr2:36375180-36375486	A549	lung:	n/a	n/a
46	CEBPB	chr2:36374848-36374960	HepG2	liver:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
47	CEBPB	chr2:36374813-36375491	IMR90	lung:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
48	CEBPB	chr2:36395379-36395613	A549	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
49	CEBPB	chr2:36497871-36498193	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr2:36449673-36449993	H1-hESC	embryonic stem cell:	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	GM12891	blood:	n/a
2	chr2:36406592-36406642	BE2_C	brain:	n/a
3	chr2:36557755-36557805	HAEpiC	amniotic membrane:	n/a
4	chr2:36557755-36557805	HRPEpiC	eye:	n/a
5	chr2:36467699-36467749	ECC-1	luminal epithelium:	n/a
6	chr2:36467699-36467749	GM12892	blood:	n/a
7	chr2:36406592-36406642	BJ	skin:	n/a
8	chr2:36565096-36565146	HIPEpiC	eye:	n/a
9	chr2:36467699-36467749	HRPEpiC	eye:	n/a
10	chr2:36557755-36557805	SK-N-SH	brain:	n/a
11	chr2:36467699-36467749	HL-60	blood:	n/a
12	chr2:36557755-36557805	ProgFib	skin:	n/a
13	chr2:36441749-36441799	NH-A	brain:	n/a
14	chr2:36406592-36406642	HCPEpiC	choroid plexus:	n/a
15	chr2:36467699-36467749	U87	brain:	n/a
16	chr2:36557755-36557805	PFSK-1	brain:	n/a
17	chr2:36441749-36441799	CMK	blood:	n/a
18	chr2:36467699-36467749	SK-N-MC	brain:	n/a
19	chr2:36406592-36406642	A549	lung:	n/a
20	chr2:36441749-36441799	LNCaP	prostate:	n/a
21	chr2:36441749-36441799	SAEC	small airway:	n/a
22	chr2:36441749-36441799	SKMC	muscle:	n/a
23	chr2:36467699-36467749	HCT-116	colon:	n/a
24	chr2:36406592-36406642	AG10803	skin:	n/a
25	chr2:36565096-36565146	GM12891	blood:	n/a
26	chr2:36565096-36565146	IMR90	lung:	fetal
27	chr2:36557755-36557805	AG04449	skin:	fetal
28	chr2:36441749-36441799	PrEC	prostate:	n/a
29	chr2:36406592-36406642	HRCEpiC	kidney:	n/a
30	chr2:36406592-36406642	H1-hESC	embryonic stem cell:	embryo
31	chr2:36441749-36441799	HCF	heart:	n/a
32	chr2:36467699-36467749	ProgFib	skin:	n/a
33	chr2:36467699-36467749	MCF10A-Er-Src	breast:	n/a
34	chr2:36565096-36565146	ECC-1	luminal epithelium:	n/a
35	chr2:36565096-36565146	SAEC	small airway:	n/a
36	chr2:36441749-36441799	HRPEpiC	eye:	n/a
37	chr2:36467699-36467749	Hepatocyte	liver:	n/a
38	chr2:36406592-36406642	NB4	blood:	n/a
39	chr2:36406592-36406642	GM12878	blood:	n/a
40	chr2:36557755-36557805	HNPCEpiC	eye:	n/a
41	chr2:36565096-36565146	GM12892	blood:	n/a
42	chr2:36406592-36406642	HEEpiC	esophagus:	n/a
43	chr2:36467699-36467749	HPAEpiC	pulmonary alveolar:	n/a
44	chr2:36441749-36441799	A549	lung:	n/a
45	chr2:36565096-36565146	AG04450	lung:	fetal
46	chr2:36441749-36441799	PANC-1	pancreas:	n/a
47	chr2:36406592-36406642	NH-A	brain:	n/a
48	chr2:36467699-36467749	HNPCEpiC	eye:	n/a
49	chr2:36467699-36467749	LNCaP	prostate:	n/a
50	chr2:36441749-36441799	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
2	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
3	chr2:36463029..36465414-chr20:47894852..47896594,2	K562	blood:
4	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
5	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
6	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
7	chr2:36569689..36572932-chr2:36575807..36579721,3	K562	blood:
8	chr2:36561664..36563772-chr2:36823426..36826394,2	MCF-7	breast:
9	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
10	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
11	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
12	chr2:36198079..36198752-chr2:36549195..36549978,3	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
ENSG00000171055	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000209042	chromatin interactions

Extended variants
information (count: 7400 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7400 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4670532	chr2:36346005-36346006	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113774755	chr2:36346052-36346053	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs377471249	chr2:36346067-36346068	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs537162168	chr2:36346085-36346086	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs562147341	chr2:36346172-36346173	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs529279669	chr2:36346173-36346174	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs372244407	chr2:36346191-36346192	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs77354513	chr2:36346239-36346240	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs559875054	chr2:36346250-36346251	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs533423527	chr2:36346267-36346268	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs527624899	chr2:36346272-36346273	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs570118921	chr2:36346278-36346279	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs537782742	chr2:36346320-36346321	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs549390239	chr2:36346322-36346323	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs188653406	chr2:36346328-36346329	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs535075763	chr2:36346387-36346388	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs542649494	chr2:36349455-36349456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72867369	chr2:36349462-36349463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531355191	chr2:36349475-36349476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528212075	chr2:36349482-36349483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4670533	chr2:36349485-36349486	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564957621	chr2:36349584-36349585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532328662	chr2:36349608-36349609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372006697	chr2:36349630-36349631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191696221	chr2:36349634-36349635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541521338	chr2:36349637-36349638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559449923	chr2:36349678-36349679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72867370	chr2:36349719-36349720	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs529891221	chr2:36349735-36349736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548198639	chr2:36349776-36349777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184061101	chr2:36349818-36349819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189654535	chr2:36349830-36349831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559007490	chr2:36349849-36349850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146370764	chr2:36349850-36349851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs180721769	chr2:36349856-36349857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs72867371	chr2:36349864-36349865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556437049	chr2:36349899-36349900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575235765	chr2:36349932-36349933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4670534	chr2:36349933-36349934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542507931	chr2:36349941-36349942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569153280	chr2:36349948-36349949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72867373	chr2:36349954-36349955	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs185980920	chr2:36350093-36350094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564981275	chr2:36350162-36350163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532067738	chr2:36350187-36350188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190626403	chr2:36350201-36350202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116988377	chr2:36350232-36350233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561144155	chr2:36350234-36350235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371546510	chr2:36350241-36350242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560162058	chr2:36350264-36350265	Enhancers Weak transcription	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:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36345600-36346400	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr2:36349400-36350200	Enhancers	Fetal Brain Male	brain
3	chr2:36350200-36350400	Enhancers	Brain Germinal Matrix	brain
4	chr2:36350200-36354000	Weak transcription	Fetal Brain Male	brain
5	chr2:36350800-36353200	Weak transcription	Brain Germinal Matrix	brain
6	chr2:36352600-36353200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:36352600-36353600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:36353200-36354000	Enhancers	Brain Germinal Matrix	brain
9	chr2:36353600-36354400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:36354000-36354400	Weak transcription	Brain Germinal Matrix	brain
11	chr2:36354000-36355200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr2:36354000-36355400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr2:36354000-36356800	Enhancers	Fetal Brain Male	brain
14	chr2:36354400-36356200	Enhancers	Brain Germinal Matrix	brain
15	chr2:36354800-36355000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:36354800-36356200	Enhancers	Fetal Brain Female	brain
17	chr2:36355200-36357400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr2:36355400-36355800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr2:36355800-36356000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:36356000-36357600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:36356200-36357200	Weak transcription	Fetal Brain Female	brain
22	chr2:36356200-36357600	Weak transcription	Brain Germinal Matrix	brain
23	chr2:36357400-36357600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:36357400-36357600	Enhancers	Fetal Brain Female	brain
25	chr2:36357600-36357800	Enhancers	Brain Germinal Matrix	brain
26	chr2:36357600-36358000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr2:36357600-36360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:36358000-36360200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:36360200-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr2:36360800-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:36364400-36365200	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr2:36364400-36365200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr2:36364600-36365000	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr2:36364600-36365200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr2:36364600-36365200	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr2:36364600-36365200	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr2:36364600-36365200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr2:36364600-36365400	Enhancers	Primary T cells from cord blood	blood
39	chr2:36364600-36365400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr2:36364800-36365200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr2:36364800-36365200	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr2:36364800-36365200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr2:36364800-36365200	Enhancers	Thymus	Thymus
44	chr2:36364800-36366000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr2:36365600-36365800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr2:36365600-36367200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:36365800-36366400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr2:36366200-36366800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr2:36366400-36367600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr2:36366600-36367000	Enhancers	Fetal Kidney	kidney

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