Variant report

Variant	esv2757792
Chromosome Location	chr2:36243452-36590658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2617)
CpG islands
(count:1348)
Chromatin interactive
region (count:43)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2617 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

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	chr2:36584228-36585957	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:36587905-36588624	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:36579092-36580173	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:36566092-36566413	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:36579218-36579449	K562	blood:	n/a	n/a
7	ARID3A	chr2:36586218-36586821	HepG2	liver:	n/a	chr2:36586337-36586352
8	ARID3A	chr2:36582582-36583062	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:36556942-36557316	HepG2	liver:	n/a	chr2:36557242-36557258
10	ATF2	chr2:36473245-36473881	GM12878	blood:	n/a	n/a
11	ATF2	chr2:36584241-36584669	GM12878	blood:	n/a	n/a
12	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
13	ATF2	chr2:36497853-36498342	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr2:36473354-36473889	GM12878	blood:	n/a	n/a
15	ATF3	chr2:36584230-36585449	A549	lung:	n/a	n/a
16	BACH1	chr2:36545626-36545719	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:36582877-36583263	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:36583875-36584225	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:36579889-36580104	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr2:36417402-36417520	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr2:36246312-36246349	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr2:36473528-36473788	GM12878	blood:	n/a	n/a
23	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
24	BATF	chr2:36467483-36467862	GM12878	blood:	n/a	n/a
25	BATF	chr2:36564561-36564770	GM12878	blood:	n/a	n/a
26	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
27	BATF	chr2:36474136-36474343	GM12878	blood:	n/a	chr2:36474255-36474266
28	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
29	BCL11A	chr2:36497933-36498242	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr2:36506762-36507002	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr2:36473409-36473790	GM12878	blood:	n/a	chr2:36473585-36473594
32	BCL3	chr2:36565737-36566479	A549	lung:	n/a	n/a
33	BCL3	chr2:36583995-36585806	A549	lung:	n/a	n/a
34	BCL3	chr2:36473447-36473808	GM12878	blood:	n/a	chr2:36473585-36473594
35	BCL3	chr2:36584056-36585850	A549	lung:	n/a	n/a
36	BCLAF1	chr2:36473380-36473879	GM12878	blood:	n/a	chr2:36473585-36473594
37	BCLAF1	chr2:36467548-36468268	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:36584014-36585232	HepG2	liver:	n/a	n/a
39	BHLHE40	chr2:36583537-36583705	A549	lung:	n/a	n/a
40	BHLHE40	chr2:36579302-36579369	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:36583466-36583788	HepG2	liver:	n/a	n/a
42	BHLHE40	chr2:36583441-36583816	GM12878	blood:	n/a	chr2:36583777-36583793
43	BHLHE40	chr2:36584374-36584709	GM12878	blood:	n/a	n/a
44	BHLHE40	chr2:36580084-36580135	GM12878	blood:	n/a	n/a
45	BHLHE40	chr2:36411001-36411307	HepG2	liver:	n/a	n/a
46	BRCA1	chr2:36579935-36579958	HepG2	liver:	n/a	n/a
47	BRCA1	chr2:36582485-36582568	HepG2	liver:	n/a	n/a
48	BRCA1	chr2:36473771-36473792	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr2:36584807-36585251	HepG2	liver:	n/a	n/a
50	BRCA1	chr2:36584394-36585476	Hela-S3	cervix:	n/a	n/a

(count:1348 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36588933-36588983	HEEpiC	esophagus:	n/a
2	chr2:36579318-36579368	HepG2	liver:	n/a
3	chr2:36588933-36588983	NT2-D1	testis:	n/a
4	chr2:36565096-36565146	HRPEpiC	eye:	n/a
5	chr2:36584021-36584071	Jurkat	blood:	n/a
6	chr2:36582038-36582088	SKMC	muscle:	n/a
7	chr2:36588933-36588983	HEEpiC	esophagus:	n/a
8	chr2:36579318-36579368	HepG2	liver:	n/a
9	chr2:36588933-36588983	NT2-D1	testis:	n/a
10	chr2:36565096-36565146	HRPEpiC	eye:	n/a
11	chr2:36584021-36584071	Jurkat	blood:	n/a
12	chr2:36582038-36582088	SKMC	muscle:	n/a
13	chr2:36582293-36582343	HRCEpiC	kidney:	n/a
14	chr2:36565096-36565146	HepG2	liver:	n/a
15	chr2:36584699-36584749	SAEC	small airway:	n/a
16	chr2:36582038-36582088	Jurkat	blood:	n/a
17	chr2:36584594-36584644	HRPEpiC	eye:	n/a
18	chr2:36565096-36565146	CMK	blood:	n/a
19	chr2:36582293-36582343	ECC-1	luminal epithelium:	n/a
20	chr2:36579318-36579368	LNCaP	prostate:	n/a
21	chr2:36589883-36589933	AG04450	lung:	fetal
22	chr2:36557755-36557805	HCM	heart:	n/a
23	chr2:36582144-36582194	SAEC	small airway:	n/a
24	chr2:36589883-36589933	NHDF-neo	bronchial:	n/a
25	chr2:36583600-36583650	NB4	blood:	n/a
26	chr2:36467699-36467749	HCF	heart:	n/a
27	chr2:36584594-36584644	HNPCEpiC	eye:	n/a
28	chr2:36582931-36582981	SAEC	small airway:	n/a
29	chr2:36582931-36582981	T-47D	breast:	n/a
30	chr2:36584981-36585031	NH-A	brain:	n/a
31	chr2:36588933-36588983	PANC-1	pancreas:	n/a
32	chr2:36584699-36584749	Caco-2	colon:	n/a
33	chr2:36441749-36441799	HNPCEpiC	eye:	n/a
34	chr2:36583600-36583650	U87	brain:	n/a
35	chr2:36582293-36582343	Caco-2	colon:	n/a
36	chr2:36582293-36582343	A549	lung:	n/a
37	chr2:36583117-36583167	NT2-D1	testis:	n/a
38	chr2:36584021-36584071	ProgFib	skin:	n/a
39	chr2:36584021-36584071	PrEC	prostate:	n/a
40	chr2:36582903-36582953	HRPEpiC	eye:	n/a
41	chr2:36582398-36582448	AG09319	gingival:	n/a
42	chr2:36584699-36584749	HL-60	blood:	n/a
43	chr2:36565096-36565146	PrEC	prostate:	n/a
44	chr2:36557755-36557805	GM06990	blood:	n/a
45	chr2:36583117-36583167	K562	blood:	n/a
46	chr2:36586710-36586760	AG10803	skin:	n/a
47	chr2:36582293-36582343	GM06990	blood:	n/a
48	chr2:36588933-36588983	T-47D	breast:	n/a
49	chr2:36584021-36584071	Hela-S3	cervix:	n/a
50	chr2:36588933-36588983	K562	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:36579120..36579851-chr2:36890803..36891518,3	MCF-7	breast:
2	chr2:36576108..36578939-chr2:36582140..36585119,3	MCF-7	breast:
3	chr2:36578991..36579848-chr2:36873541..36874070,2	K562	blood:
4	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
5	chr2:36262623..36264860-chr2:36265182..36267594,2	K562	blood:
6	chr2:36579295..36579845-chr2:36891074..36891911,3	K562	blood:
7	chr2:36243496..36245168-chr2:36248339..36251225,2	K562	blood:
8	chr2:36585022..36585655-chr7:103237622..103238142,2	MCF-7	breast:
9	chr2:36581144..36585281-chr2:36586722..36590613,9	MCF-7	breast:
10	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
11	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
12	chr2:36586071..36588141-chr2:36602497..36605299,2	MCF-7	breast:
13	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
14	chr2:36579197..36579769-chr2:36686712..36687259,2	MCF-7	breast:
15	chr2:36579541..36582234-chr2:36891147..36893577,3	MCF-7	breast:
16	chr2:36579071..36579733-chr2:36734184..36735079,2	MCF-7	breast:
17	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
18	chr2:36463029..36465414-chr20:47894852..47896594,2	K562	blood:
19	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
20	chr2:36586047..36587747-chr2:36587978..36589584,2	MCF-7	breast:
21	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
22	chr2:36262623..36264860-chr2:36265182..36267594,2	K562	blood:
23	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
24	chr2:36582124..36584781-chr2:36595194..36598033,3	MCF-7	breast:
25	chr2:36579431..36580979-chr2:36581786..36583464,2	MCF-7	breast:
26	chr2:36587314..36589813-chr2:36643724..36646171,2	MCF-7	breast:
27	chr2:36198095..36199022-chr2:36584804..36585700,2	MCF-7	breast:
28	chr2:36579337..36579853-chr2:36872696..36873518,2	K562	blood:
29	chr2:36585288..36588127-chr2:36593960..36595657,2	MCF-7	breast:
30	chr2:36582902..36585503-chr2:36823410..36825462,3	MCF-7	breast:
31	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
32	chr2:36579342..36579861-chr2:37012057..37012873,2	K562	blood:
33	chr2:36579157..36579830-chr2:36734235..36735159,5	MCF-7	breast:
34	chr2:36243496..36245168-chr2:36248339..36251225,2	K562	blood:
35	chr2:36586047..36587747-chr2:36587978..36589584,2	MCF-7	breast:
36	chr11:75052700..75053203-chr2:36584480..36585374,2	MCF-7	breast:
37	chr2:36569689..36572932-chr2:36575807..36579721,3	K562	blood:
38	chr2:36587591..36589572-chr2:36660142..36662034,2	MCF-7	breast:
39	chr2:36581644..36585884-chr2:36589453..36593565,5	MCF-7	breast:
40	chr2:36579116..36579764-chr2:36686740..36687372,2	MCF-7	breast:
41	chr2:36587815..36589906-chr2:36591154..36593717,2	MCF-7	breast:
42	chr2:36569689..36572932-chr2:36575807..36579721,3	K562	blood:
43	chr2:36561664..36563772-chr2:36823426..36826394,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-1	chr2:36581908-36582124	XLOC_002048
2	lnc-AC007401.2.1-5	chr2:36526531-36526973	NONHSAT070076
3	lnc-AC007401.2.1-1	chr2:36582231-36582713	NR_037631
4	lnc-AC007401.2.1-1	chr2:36581892-36582257	ENSG00000260025.1
5	lnc-AC007401.2.1-1	chr2:36581892-36582124	NR_037631
6	lnc-AC007401.2.1-1	chr2:36582231-36582636	XLOC_002048
7	lnc-AC007401.2.1-1	chr2:36581478-36582124	NONHSAT070077
8	lnc-AC007401.2.1-1	chr2:36582231-36582763	NONHSAT070077
9	lnc-AC007401.2.1-1	chr2:36582262-36582739	NONHSAT070079
10	lnc-AC007401.2.1-1	chr2:36581895-36582124	NONHSAT070079

No data

Variant related genes	Relation type
CRIM1	TF binding region
ENSG00000260025	TF binding region
ENSG00000233752	TF binding region
CRIM1	CpG island
ENSG00000260025	CpG island
ENSG00000233752	CpG island
ENSG00000209042	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000150938	chromatin interactions
ENSG00000260025	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000171055	chromatin interactions
RPRD2	miRNA target sites

Extended variants
information (count: 9631 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:9631 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563228063	chr2:36253666-36253667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112504746	chr2:36253669-36253670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114169480	chr2:36253683-36253684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1489157	chr2:36253750-36253751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561177107	chr2:36253784-36253785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115341531	chr2:36253805-36253806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547040667	chr2:36253816-36253817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370753311	chr2:36253834-36253835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75955053	chr2:36253835-36253836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140457101	chr2:36253841-36253842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563802362	chr2:36253878-36253879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538552864	chr2:36253934-36253935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551097625	chr2:36253946-36253947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114527366	chr2:36253977-36253978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536454512	chr2:36254019-36254020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372049132	chr2:36254046-36254047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554707143	chr2:36254047-36254048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531252284	chr2:36254056-36254057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527339975	chr2:36254098-36254099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556612699	chr2:36254099-36254100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578179755	chr2:36254120-36254121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558730221	chr2:36254125-36254126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534248742	chr2:36254157-36254158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545323826	chr2:36254159-36254160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192504940	chr2:36254207-36254208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546123277	chr2:36254208-36254209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577606859	chr2:36254215-36254216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13030155	chr2:36254249-36254250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111646028	chr2:36254273-36254274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs13391203	chr2:36254305-36254306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369985682	chr2:36254349-36254350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185066979	chr2:36254416-36254417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189001346	chr2:36254427-36254428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75495114	chr2:36254431-36254432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149721903	chr2:36254453-36254454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145243586	chr2:36254459-36254460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547190660	chr2:36254471-36254472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs62132715	chr2:36254511-36254512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs56983655	chr2:36254555-36254556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528266056	chr2:36254599-36254600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75383507	chr2:36254624-36254625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564990443	chr2:36254630-36254631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181679599	chr2:36254661-36254662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115187049	chr2:36254686-36254687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569045705	chr2:36254710-36254711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186177728	chr2:36254740-36254741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548251093	chr2:36254821-36254822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10495861	chr2:36254823-36254824	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs534086961	chr2:36254873-36254874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559207077	chr2:36254891-36254892	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1823 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36253600-36253800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:36253800-36254400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:36254400-36255600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:36254800-36255200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:36269400-36271600	Enhancers	Brain Hippocampus Middle	brain
6	chr2:36269800-36271200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:36270600-36270800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:36270600-36270800	Enhancers	Brain Angular Gyrus	brain
9	chr2:36270600-36271000	Enhancers	Brain Cingulate Gyrus	brain
10	chr2:36270800-36271400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:36271400-36272000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:36271600-36272200	Enhancers	Duodenum Mucosa	Duodenum
13	chr2:36271600-36273000	Enhancers	Fetal Intestine Small	intestine
14	chr2:36280200-36280600	Enhancers	HepG2	liver
15	chr2:36284600-36284800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:36284600-36285800	Enhancers	Primary T cells from cord blood	blood
17	chr2:36284600-36286400	Enhancers	HUVEC	blood vessel
18	chr2:36284800-36286000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr2:36284800-36286200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:36284800-36287600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr2:36284800-36287800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:36284800-36287800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr2:36285000-36285400	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr2:36285200-36285400	Enhancers	Primary hematopoietic stem cells	blood
25	chr2:36285200-36285400	Enhancers	Fetal Intestine Small	intestine
26	chr2:36285200-36285600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr2:36285200-36286200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr2:36285200-36287800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr2:36285200-36288000	Enhancers	Fetal Intestine Large	intestine
30	chr2:36285400-36286200	Weak transcription	Primary hematopoietic stem cells	blood
31	chr2:36285400-36286200	Weak transcription	Fetal Intestine Small	intestine
32	chr2:36285600-36286800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr2:36285800-36286000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr2:36285800-36286200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:36286200-36286400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:36286200-36286400	Enhancers	Small Intestine	intestine
37	chr2:36286200-36286400	Enhancers	GM12878-XiMat	blood
38	chr2:36286200-36287000	Enhancers	Duodenum Mucosa	Duodenum
39	chr2:36286200-36287000	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr2:36286200-36287000	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr2:36286200-36287600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr2:36286200-36287800	Enhancers	Fetal Intestine Small	intestine
43	chr2:36286200-36288000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr2:36286200-36288000	Enhancers	Primary hematopoietic stem cells	blood
45	chr2:36286400-36286800	Weak transcription	GM12878-XiMat	blood
46	chr2:36286400-36287200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:36286400-36287400	Weak transcription	Small Intestine	intestine
48	chr2:36286600-36287600	Enhancers	Primary B cells from cord blood	blood
49	chr2:36286800-36287400	ZNF genes & repeats	GM12878-XiMat	blood
50	chr2:36286800-36287600	Enhancers	Primary monocytes fromperipheralblood	blood

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