Variant report

Variant	esv34222
Chromosome Location	chr2:36309662-36569049
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	chr2:36473245-36473881	GM12878	blood:	n/a	n/a
5	ATF2	chr2:36497853-36498342	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:36473354-36473889	GM12878	blood:	n/a	n/a
7	ATF2	chr2:36374728-36375202	GM12878	blood:	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	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
12	BATF	chr2:36473528-36473788	GM12878	blood:	n/a	n/a
13	BATF	chr2:36467483-36467862	GM12878	blood:	n/a	n/a
14	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
15	BATF	chr2:36474136-36474343	GM12878	blood:	n/a	chr2:36474255-36474266
16	BCL11A	chr2:36497933-36498242	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
20	BCL3	chr2:36473447-36473808	GM12878	blood:	n/a	chr2:36473585-36473594
21	BCL3	chr2:36565737-36566479	A549	lung:	n/a	n/a
22	BCLAF1	chr2:36467548-36468268	GM12878	blood:	n/a	n/a
23	BCLAF1	chr2:36473380-36473879	GM12878	blood:	n/a	chr2:36473585-36473594
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	chr2:36374793-36375473	Hela-S3	cervix:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
28	CEBPB	chr2:36380814-36381038	IMR90	lung:	n/a	chr2:36380974-36380985
29	CEBPB	chr2:36556053-36556379	IMR90	lung:	n/a	chr2:36556209-36556220
30	CEBPB	chr2:36514534-36514969	IMR90	lung:	n/a	chr2:36514780-36514791
31	CEBPB	chr2:36556964-36557296	A549	lung:	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	chr2:36556951-36557349	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:36354969-36355117	HepG2	liver:	n/a	chr2:36355034-36355045
35	CEBPB	chr2:36556740-36557429	A549	lung:	n/a	n/a
36	CEBPB	chr2:36514610-36514947	A549	lung:	n/a	chr2:36514780-36514791
37	CEBPB	chr2:36375217-36375486	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:36395338-36395598	Hela-S3	cervix:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
39	CEBPB	chr2:36374848-36374960	HepG2	liver:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
40	CEBPB	chr2:36548842-36549024	A549	lung:	n/a	n/a
41	CEBPB	chr2:36556102-36556393	A549	lung:	n/a	chr2:36556209-36556220
42	CEBPB	chr2:36548793-36548993	HepG2	liver:	n/a	n/a
43	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
44	CEBPB	chr2:36395324-36395659	HepG2	liver:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
45	CEBPB	chr2:36567018-36567360	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:36437530-36437813	HepG2	liver:	n/a	chr2:36437627-36437638
47	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
48	CEBPB	chr2:36565742-36566503	A549	lung:	n/a	n/a
49	CEBPB	chr2:36434759-36434959	IMR90	lung:	n/a	chr2:36434830-36434841
50	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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36406592-36406642	MCF-7	breast:	n/a
2	chr2:36467699-36467749	AoSMC	blood vessel:	n/a
3	chr2:36557755-36557805	AG04449	skin:	fetal
4	chr2:36406592-36406642	ProgFib	skin:	n/a
5	chr2:36557755-36557805	GM12878	blood:	n/a
6	chr2:36565096-36565146	AG04449	skin:	fetal
7	chr2:36565096-36565146	Hela-S3	cervix:	n/a
8	chr2:36467699-36467749	HRE	kidney:	n/a
9	chr2:36565096-36565146	BE2_C	brain:	n/a
10	chr2:36565096-36565146	NH-A	brain:	n/a
11	chr2:36406592-36406642	HCM	heart:	n/a
12	chr2:36565096-36565146	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:36406592-36406642	HIPEpiC	eye:	n/a
14	chr2:36565096-36565146	AG09309	skin:	n/a
15	chr2:36406592-36406642	U87	brain:	n/a
16	chr2:36565096-36565146	H1-hESC	embryonic stem cell:	embryo
17	chr2:36557755-36557805	H1-hESC	embryonic stem cell:	embryo
18	chr2:36467699-36467749	K562	blood:	n/a
19	chr2:36565096-36565146	LNCaP	prostate:	n/a
20	chr2:36441749-36441799	MCF10A-Er-Src	breast:	n/a
21	chr2:36441749-36441799	HMEC	breast:	n/a
22	chr2:36565096-36565146	NB4	blood:	n/a
23	chr2:36565096-36565146	GM12878	blood:	n/a
24	chr2:36557755-36557805	Hepatocyte	liver:	n/a
25	chr2:36406592-36406642	AG04449	skin:	fetal
26	chr2:36565096-36565146	SKMC	muscle:	n/a
27	chr2:36565096-36565146	Caco-2	colon:	n/a
28	chr2:36565096-36565146	AG04450	lung:	fetal
29	chr2:36441749-36441799	GM12878	blood:	n/a
30	chr2:36406592-36406642	NHBE	bronchial:	n/a
31	chr2:36467699-36467749	Hela-S3	cervix:	n/a
32	chr2:36467699-36467749	PFSK-1	brain:	n/a
33	chr2:36406592-36406642	HAEpiC	amniotic membrane:	n/a
34	chr2:36565096-36565146	HCF	heart:	n/a
35	chr2:36467699-36467749	HEEpiC	esophagus:	n/a
36	chr2:36406592-36406642	HL-60	blood:	n/a
37	chr2:36557755-36557805	GM06990	blood:	n/a
38	chr2:36557755-36557805	NB4	blood:	n/a
39	chr2:36406592-36406642	NT2-D1	testis:	n/a
40	chr2:36441749-36441799	HL-60	blood:	n/a
41	chr2:36441749-36441799	ProgFib	skin:	n/a
42	chr2:36565096-36565146	AoSMC	blood vessel:	n/a
43	chr2:36557755-36557805	HCM	heart:	n/a
44	chr2:36467699-36467749	HCM	heart:	n/a
45	chr2:36441749-36441799	AG09319	gingival:	n/a
46	chr2:36467699-36467749	HUVEC	blood vessel:	n/a
47	chr2:36441749-36441799	NH-A	brain:	n/a
48	chr2:36406592-36406642	GM12878	blood:	n/a
49	chr2:36565096-36565146	U87	brain:	n/a
50	chr2:36406592-36406642	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
2	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
3	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
4	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
5	chr2:36561664..36563772-chr2:36823426..36826394,2	MCF-7	breast:
6	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
7	chr2:36463029..36465414-chr20:47894852..47896594,2	K562	blood:
8	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
9	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
10	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
11	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
ENSG00000171055	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000177410	chromatin interactions

Extended variants
information (count: 7468 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7468 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555253817	chr2:36314049-36314050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573591202	chr2:36314051-36314052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1995912	chr2:36314056-36314057	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559297746	chr2:36314066-36314067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375145083	chr2:36314083-36314084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368212348	chr2:36314168-36314169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558552992	chr2:36314233-36314234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577107032	chr2:36314243-36314244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545184304	chr2:36314257-36314258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563771660	chr2:36314264-36314265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531014347	chr2:36314271-36314272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557259566	chr2:36314275-36314276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569479393	chr2:36314318-36314319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142205443	chr2:36314322-36314323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs151226251	chr2:36314337-36314338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528791719	chr2:36314364-36314365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs72867308	chr2:36314367-36314368	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs565696009	chr2:36314412-36314413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539391950	chr2:36314469-36314470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557571872	chr2:36314488-36314489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190715595	chr2:36314531-36314532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75926319	chr2:36314538-36314539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559754781	chr2:36318403-36318404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142169891	chr2:36318405-36318406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551938819	chr2:36318469-36318470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115143871	chr2:36318492-36318493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184115636	chr2:36318493-36318494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111748096	chr2:36318520-36318521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568076760	chr2:36318583-36318584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535413271	chr2:36318588-36318589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553588337	chr2:36318590-36318591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57834221	chr2:36318635-36318636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549691548	chr2:36318657-36318658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs305165	chr2:36318689-36318690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201638319	chr2:36318697-36318698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563860302	chr2:36318705-36318706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543329928	chr2:36318712-36318713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188070462	chr2:36318722-36318723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191169079	chr2:36318746-36318747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147405525	chr2:36318747-36318748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373783498	chr2:36318748-36318749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541378403	chr2:36318803-36318804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546172442	chr2:36318835-36318836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183647609	chr2:36318847-36318848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs578044622	chr2:36318853-36318854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545298771	chr2:36318854-36318855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563855571	chr2:36318884-36318885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531091386	chr2:36318896-36318897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549719392	chr2:36318920-36318921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190197435	chr2:36318952-36318953	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:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36314000-36314600	Enhancers	Fetal Brain Female	brain
2	chr2:36318400-36319000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:36319000-36319800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:36319400-36320000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:36319800-36322800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:36324000-36324400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr2:36324400-36324600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:36345600-36346400	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr2:36349400-36350200	Enhancers	Fetal Brain Male	brain
10	chr2:36350200-36350400	Enhancers	Brain Germinal Matrix	brain
11	chr2:36350200-36354000	Weak transcription	Fetal Brain Male	brain
12	chr2:36350800-36353200	Weak transcription	Brain Germinal Matrix	brain
13	chr2:36352600-36353200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:36352600-36353600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:36353200-36354000	Enhancers	Brain Germinal Matrix	brain
16	chr2:36353600-36354400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:36354000-36354400	Weak transcription	Brain Germinal Matrix	brain
18	chr2:36354000-36355200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr2:36354000-36355400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:36354000-36356800	Enhancers	Fetal Brain Male	brain
21	chr2:36354400-36356200	Enhancers	Brain Germinal Matrix	brain
22	chr2:36354800-36355000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:36354800-36356200	Enhancers	Fetal Brain Female	brain
24	chr2:36355200-36357400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr2:36355400-36355800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:36355800-36356000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:36356000-36357600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:36356200-36357200	Weak transcription	Fetal Brain Female	brain
29	chr2:36356200-36357600	Weak transcription	Brain Germinal Matrix	brain
30	chr2:36357400-36357600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr2:36357400-36357600	Enhancers	Fetal Brain Female	brain
32	chr2:36357600-36357800	Enhancers	Brain Germinal Matrix	brain
33	chr2:36357600-36358000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr2:36357600-36360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:36358000-36360200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr2:36360200-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr2:36360800-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:36364400-36365200	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr2:36364400-36365200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr2:36364600-36365000	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr2:36364600-36365200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr2:36364600-36365200	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr2:36364600-36365200	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr2:36364600-36365200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr2:36364600-36365400	Enhancers	Primary T cells from cord blood	blood
46	chr2:36364600-36365400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr2:36364800-36365200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr2:36364800-36365200	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr2:36364800-36365200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:36364800-36365200	Enhancers	Thymus	Thymus

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