Variant report

Variant	esv3693430
Chromosome Location	chr2:152648677-152681200
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:564)
CpG islands
(count:61)
Chromatin interactive
region (count:48)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:152664778-152665235	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:152656261-152657191	K562	blood:	n/a	n/a
3	ARID3A	chr2:152661921-152662105	K562	blood:	n/a	n/a
4	ARID3A	chr2:152672556-152673120	K562	blood:	n/a	n/a
5	ARID3A	chr2:152664783-152665204	K562	blood:	n/a	n/a
6	ATF1	chr2:152672620-152672949	K562	blood:	n/a	n/a
7	ATF1	chr2:152656333-152656862	K562	blood:	n/a	n/a
8	ATF3	chr2:152656365-152656773	K562	blood:	n/a	n/a
9	BACH1	chr2:152656498-152656609	K562	blood:	n/a	n/a
10	BATF	chr2:152676485-152676813	GM12878	blood:	n/a	chr2:152676624-152676635
11	BATF	chr2:152676400-152676876	GM12878	blood:	n/a	chr2:152676624-152676635
12	BHLHE40	chr2:152672682-152672894	K562	blood:	n/a	n/a
13	BHLHE40	chr2:152649232-152649399	K562	blood:	n/a	n/a
14	BHLHE40	chr2:152656385-152656785	K562	blood:	n/a	n/a
15	CBX3	chr2:152656270-152656943	K562	blood:	n/a	n/a
16	CBX3	chr2:152650950-152651471	HCT-116	colon:	n/a	n/a
17	CBX3	chr2:152651032-152651327	HCT-116	colon:	n/a	n/a
18	CBX3	chr2:152672358-152673052	K562	blood:	n/a	n/a
19	CCNT2	chr2:152656356-152656963	K562	blood:	n/a	n/a
20	CCNT2	chr2:152673249-152673688	K562	blood:	n/a	n/a
21	CCNT2	chr2:152672665-152673014	K562	blood:	n/a	n/a
22	CEBPB	chr2:152660146-152660561	K562	blood:	n/a	chr2:152660262-152660273 chr2:152660262-152660275 chr2:152660262-152660273
23	CEBPB	chr2:152653241-152653634	ECC-1	luminal epithelium:	n/a	chr2:152653419-152653432
24	CEBPB	chr2:152656388-152656760	K562	blood:	n/a	n/a
25	CEBPB	chr2:152652371-152652715	A549	lung:	n/a	n/a
26	CEBPB	chr2:152652374-152652727	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:152652367-152652743	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:152672657-152672907	K562	blood:	n/a	n/a
29	CEBPB	chr2:152652390-152652705	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:152656248-152656794	K562	blood:	n/a	n/a
31	CEBPB	chr2:152652349-152652765	A549	lung:	n/a	n/a
32	CEBPB	chr2:152652384-152652737	K562	blood:	n/a	n/a
33	CEBPB	chr2:152652375-152652731	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:152661972-152662132	K562	blood:	n/a	n/a
35	CEBPB	chr2:152652320-152652792	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr2:152661982-152662147	A549	lung:	n/a	n/a
37	CEBPD	chr2:152656001-152656883	K562	blood:	n/a	n/a
38	CEBPD	chr2:152672494-152673073	K562	blood:	n/a	n/a
39	CEBPD	chr2:152672507-152673114	K562	blood:	n/a	n/a
40	CEBPD	chr2:152656307-152656900	K562	blood:	n/a	n/a
41	CREB1	chr2:152656033-152657159	K562	blood:	n/a	n/a
42	CTCF	chr2:152664940-152665090	HPF	lung:	n/a	chr2:152665013-152665026 chr2:152665006-152665027 chr2:152665011-152665029
43	CTCF	chr2:152664925-152665143	Hela-S3	cervix:	n/a	chr2:152665013-152665026 chr2:152665006-152665027 chr2:152665011-152665029
44	CTCF	chr2:152649126-152649455	K562	blood:	n/a	chr2:152649303-152649321
45	CTCF	chr2:152664897-152665152	Medullo	brain:	n/a	chr2:152665013-152665026 chr2:152665006-152665027 chr2:152665011-152665029
46	CTCF	chr2:152664960-152665110	AG04449	skin:	n/a	chr2:152665013-152665026 chr2:152665006-152665027 chr2:152665011-152665029
47	CTCF	chr2:152664980-152665130	GM12868	blood:	n/a	chr2:152665013-152665026 chr2:152665006-152665027 chr2:152665011-152665029
48	CTCF	chr2:152649220-152649370	HFF	foreskin:	n/a	chr2:152649303-152649321
49	CTCF	chr2:152664940-152665090	HA-sp	spinal cord:	n/a	chr2:152665013-152665026 chr2:152665006-152665027 chr2:152665011-152665029
50	CTCF	chr2:152649180-152649330	GM12866	blood:	n/a	chr2:152649303-152649321

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152663031-152663081	K562	blood:	n/a
2	chr2:152663031-152663081	HRE	kidney:	n/a
3	chr2:152663031-152663081	Hepatocyte	liver:	n/a
4	chr2:152663031-152663081	AoSMC	blood vessel:	n/a
5	chr2:152663031-152663081	HEEpiC	esophagus:	n/a
6	chr2:152663031-152663081	NB4	blood:	n/a
7	chr2:152663031-152663081	HMEC	breast:	n/a
8	chr2:152663031-152663081	AG09319	gingival:	n/a
9	chr2:152663031-152663081	RPTEC	kidney:	n/a
10	chr2:152663031-152663081	HRPEpiC	eye:	n/a
11	chr2:152663031-152663081	SAEC	small airway:	n/a
12	chr2:152663031-152663081	AG10803	skin:	n/a
13	chr2:152663031-152663081	HEK293	kidney:	embryo
14	chr2:152663031-152663081	ECC-1	luminal epithelium:	n/a
15	chr2:152663031-152663081	GM06990	blood:	n/a
16	chr2:152663031-152663081	ovcar-3	ovarian:	n/a
17	chr2:152663031-152663081	PrEC	prostate:	n/a
18	chr2:152663031-152663081	PFSK-1	brain:	n/a
19	chr2:152663031-152663081	CMK	blood:	n/a
20	chr2:152663031-152663081	Hela-S3	cervix:	n/a
21	chr2:152663031-152663081	BJ	skin:	n/a
22	chr2:152663031-152663081	HepG2	liver:	n/a
23	chr2:152663031-152663081	AG04449	skin:	fetal
24	chr2:152663031-152663081	MCF10A-Er-Src	breast:	n/a
25	chr2:152663031-152663081	HUVEC	blood vessel:	n/a
26	chr2:152663031-152663081	AG04450	lung:	fetal
27	chr2:152663031-152663081	Jurkat	blood:	n/a
28	chr2:152663031-152663081	T-47D	breast:	n/a
29	chr2:152663031-152663081	NT2-D1	testis:	n/a
30	chr2:152663031-152663081	GM12892	blood:	n/a
31	chr2:152663031-152663081	U87	brain:	n/a
32	chr2:152663031-152663081	HIPEpiC	eye:	n/a
33	chr2:152663031-152663081	H1-hESC	embryonic stem cell:	embryo
34	chr2:152663031-152663081	A549	lung:	n/a
35	chr2:152663031-152663081	HCT-116	colon:	n/a
36	chr2:152663031-152663081	HNPCEpiC	eye:	n/a
37	chr2:152663031-152663081	NH-A	brain:	n/a
38	chr2:152663031-152663081	HCM	heart:	n/a
39	chr2:152663031-152663081	HAEpiC	amniotic membrane:	n/a
40	chr2:152663031-152663081	PANC-1	pancreas:	n/a
41	chr2:152663031-152663081	NHDF-neo	bronchial:	n/a
42	chr2:152663031-152663081	ProgFib	skin:	n/a
43	chr2:152663031-152663081	GM12891	blood:	n/a
44	chr2:152663031-152663081	Caco-2	colon:	n/a
45	chr2:152663031-152663081	BE2_C	brain:	n/a
46	chr2:152663031-152663081	NHBE	bronchial:	n/a
47	chr2:152663031-152663081	SK-N-SH_RA	brain:	n/a
48	chr2:152663031-152663081	GM12878	blood:	n/a
49	chr2:152663031-152663081	HCF	heart:	n/a
50	chr2:152663031-152663081	SK-N-MC	brain:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:152655681..152658497-chr2:152663463..152665219,2	K562	blood:
2	chr2:152656997..152660180-chr2:152663044..152665529,3	K562	blood:
3	chr2:152646306..152650027-chr2:152650501..152653927,4	K562	blood:
4	chr2:152649695..152652576-chr2:152683418..152685881,2	K562	blood:
5	chr2:152671480..152673477-chr2:152674012..152675938,2	K562	blood:
6	chr2:152656997..152660180-chr2:152663044..152665529,3	K562	blood:
7	chr2:152650007..152652508-chr2:152654321..152656422,3	K562	blood:
8	chr2:152655109..152656955-chr2:152681729..152684723,2	K562	blood:
9	chr2:152680613..152683339-chr2:152701936..152703952,2	K562	blood:
10	chr2:152667073..152668792-chr2:152670517..152672441,2	K562	blood:
11	chr2:152668478..152670762-chr2:152674292..152676258,2	K562	blood:
12	chr2:152670087..152672133-chr2:152680755..152682806,2	MCF-7	breast:
13	chr2:152667156..152671045-chr2:152683562..152687272,7	K562	blood:
14	chr2:152657917..152660487-chr2:152685208..152686908,2	K562	blood:
15	chr2:152650007..152652508-chr2:152654321..152656422,3	K562	blood:
16	chr2:152662842..152666419-chr2:152667793..152671423,3	K562	blood:
17	chr2:152634127..152636194-chr2:152671394..152673328,2	K562	blood:
18	chr2:152668478..152670762-chr2:152674292..152676258,2	K562	blood:
19	chr2:152664790..152667573-chr2:152691084..152693387,2	MCF-7	breast:
20	chr2:152666269..152668402-chr2:152669903..152671497,2	MCF-7	breast:
21	chr2:152644390..152647608-chr2:152655102..152657345,3	K562	blood:
22	chr2:152644348..152647772-chr2:152655102..152659949,6	K562	blood:
23	chr2:152661672..152663988-chr2:152664069..152666559,3	MCF-7	breast:
24	chr2:152658528..152660936-chr2:152662240..152664353,2	K562	blood:
25	chr2:152666269..152668402-chr2:152669903..152671497,2	MCF-7	breast:
26	chr2:152670087..152672133-chr2:152680755..152682806,2	MCF-7	breast:
27	chr2:152662842..152666419-chr2:152667793..152671423,3	K562	blood:
28	chr2:152665251..152666144-chr2:152855012..152855870,2	MCF-7	breast:
29	chr2:152655681..152658497-chr2:152663463..152665219,2	K562	blood:
30	chr2:152648527..152650395-chr2:152650501..152652844,2	K562	blood:
31	chr2:152671480..152673477-chr2:152674012..152675938,2	K562	blood:
32	chr2:152653051..152655697-chr2:152658456..152660415,2	K562	blood:
33	chr2:152667156..152669277-chr2:152683562..152686804,3	K562	blood:
34	chr2:152663598..152665100-chr2:152681522..152683558,2	K562	blood:
35	chr2:152667073..152668792-chr2:152670517..152672441,2	K562	blood:
36	chr2:152667501..152670036-chr2:152673643..152675792,3	K562	blood:
37	chr2:152639494..152642150-chr2:152659901..152662839,2	K562	blood:
38	chr2:152623919..152627757-chr2:152680404..152683778,4	K562	blood:
39	chr2:152661672..152663988-chr2:152664069..152666559,3	MCF-7	breast:
40	chr2:152658528..152660936-chr2:152662240..152664353,2	K562	blood:
41	chr2:152653051..152655697-chr2:152658456..152660415,2	K562	blood:
42	chr2:152640887..152642607-chr2:152677415..152680020,2	K562	blood:
43	chr2:152630249..152631929-chr2:152665981..152667860,2	K562	blood:
44	chr2:152505042..152505695-chr2:152664523..152665175,2	MCF-7	breast:
45	chr2:152655109..152657619-chr2:152681729..152683348,2	K562	blood:
46	chr2:152640166..152642990-chr2:152671460..152673165,2	K562	blood:
47	chr2:152667501..152670036-chr2:152673643..152675792,3	K562	blood:
48	chr2:152660681..152662473-chr2:152683493..152685563,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL5A-1	chr2:152648272-152649559	NONHSAT074964
2	lnc-RIF1-2	chr2:152652281-152653023	NONHSAT074963

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ARL5A	hsa-miR-155-5p	chr2:152658856-152658878

Variant related genes	Relation type
ARL5A	TF binding region
ARL5A	CpG island
ENSG00000162980	chromatin interactions

Extended variants
information (count: 1154 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1154 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11680834	chr2:152648677-152648678	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574232093	chr2:152648679-152648680	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs56273723	chr2:152648699-152648700	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs561740221	chr2:152648731-152648732	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs143131394	chr2:152648733-152648734	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs547394986	chr2:152648741-152648742	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs149106580	chr2:152648783-152648784	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs185964409	chr2:152648878-152648879	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs569207688	chr2:152648889-152648890	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs373374358	chr2:152648902-152648903	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs533044787	chr2:152648933-152648934	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs549395534	chr2:152648935-152648936	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs191310463	chr2:152648948-152648949	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs183053293	chr2:152649025-152649026	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs138871080	chr2:152649038-152649039	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs112522595	chr2:152649061-152649062	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs566145566	chr2:152649094-152649095	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs376635499	chr2:152649102-152649103	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs142744933	chr2:152649111-152649112	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs534226674	chr2:152649122-152649123	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs578256844	chr2:152649150-152649151	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs146965010	chr2:152649161-152649162	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs557432309	chr2:152649201-152649202	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs573937702	chr2:152649227-152649228	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs549484313	chr2:152649233-152649234	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs567683121	chr2:152649248-152649249	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs138036940	chr2:152649288-152649289	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs548325424	chr2:152649291-152649292	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs188390559	chr2:152649342-152649343	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs190541411	chr2:152649413-152649414	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs572160735	chr2:152649433-152649434	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs541256730	chr2:152649466-152649467	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs563919884	chr2:152649536-152649537	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs559870298	chr2:152649537-152649538	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs183191112	chr2:152649539-152649540	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs114398744	chr2:152649549-152649550	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs187730953	chr2:152649606-152649607	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs150512282	chr2:152649616-152649617	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs192534755	chr2:152649633-152649634	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs183690932	chr2:152649689-152649690	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs187658807	chr2:152649709-152649710	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs139936712	chr2:152649717-152649718	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs376736079	chr2:152649732-152649733	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs78092271	chr2:152649909-152649910	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192784497	chr2:152649953-152649954	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs184663306	chr2:152649981-152649982	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116596978	chr2:152650045-152650046	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs117818391	chr2:152650050-152650051	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573317700	chr2:152650134-152650135	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs202074445	chr2:152650138-152650139	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1064 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152616800-152662400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr2:152617000-152669400	Weak transcription	Gastric	stomach
3	chr2:152619000-152677400	Weak transcription	Brain Substantia Nigra	brain
4	chr2:152622200-152661800	Weak transcription	Fetal Kidney	kidney
5	chr2:152623000-152680000	Weak transcription	Spleen	Spleen
6	chr2:152623400-152658800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr2:152623400-152659000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:152623600-152659000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr2:152624000-152662600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr2:152624400-152656800	Weak transcription	HepG2	liver
11	chr2:152625400-152660000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr2:152628000-152654800	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr2:152629000-152661800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr2:152631400-152652000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr2:152631400-152667200	Weak transcription	Colon Smooth Muscle	Colon
16	chr2:152631600-152661800	Weak transcription	HMEC	breast
17	chr2:152632000-152659000	Weak transcription	NHLF	lung
18	chr2:152632200-152656400	Weak transcription	NH-A	brain
19	chr2:152632200-152679200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:152632400-152649000	Weak transcription	Osteobl	bone
21	chr2:152632600-152652000	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr2:152633000-152652200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr2:152633000-152662200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr2:152633400-152650400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr2:152634000-152665400	Weak transcription	Fetal Stomach	stomach
26	chr2:152634000-152683400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr2:152634200-152657000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:152634200-152661000	Weak transcription	A549	lung
29	chr2:152634600-152661800	Weak transcription	NHEK	skin
30	chr2:152634800-152658200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr2:152634800-152672200	Weak transcription	Right Ventricle	heart
32	chr2:152635600-152659000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr2:152636000-152662400	Weak transcription	Fetal Brain Female	brain
34	chr2:152636400-152649200	Weak transcription	GM12878-XiMat	blood
35	chr2:152636400-152659000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr2:152636400-152661800	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr2:152636600-152661600	Weak transcription	Colonic Mucosa	Colon
38	chr2:152636800-152649000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:152637000-152657400	Weak transcription	Dnd41	blood
40	chr2:152637000-152657800	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr2:152637000-152659000	Weak transcription	Fetal Brain Male	brain
42	chr2:152638200-152653200	Weak transcription	Fetal Heart	heart
43	chr2:152638600-152661800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr2:152638600-152662000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr2:152638600-152665200	Weak transcription	Pancreas	Pancrea
46	chr2:152638600-152671000	Weak transcription	Thymus	Thymus
47	chr2:152638800-152665200	Weak transcription	Fetal Intestine Small	intestine
48	chr2:152638800-152668200	Weak transcription	Lung	lung
49	chr2:152638800-152672800	Weak transcription	Aorta	Aorta
50	chr2:152639600-152659000	Weak transcription	Fetal Lung	lung

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