Variant report

Variant	nsv2751
Chromosome Location	chr2:62691264-62737131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:831)
CpG islands
(count:856)
Chromatin interactive
region (count:39)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:831 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:62728740-62729279	K562	blood:	n/a	n/a
2	ARID3A	chr2:62726572-62727203	K562	blood:	n/a	n/a
3	ARID3A	chr2:62733002-62733248	K562	blood:	n/a	n/a
4	ARID3A	chr2:62733451-62733911	K562	blood:	n/a	n/a
5	ARID3A	chr2:62694933-62695177	HepG2	liver:	n/a	n/a
6	ATF1	chr2:62732883-62733638	K562	blood:	n/a	n/a
7	ATF1	chr2:62728987-62729279	K562	blood:	n/a	n/a
8	ATF1	chr2:62699867-62700109	K562	blood:	n/a	n/a
9	ATF2	chr2:62692950-62693466	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:62692911-62693426	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:62732770-62733279	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr2:62732731-62733633	A549	lung:	n/a	chr2:62732805-62732814 chr2:62732759-62732768
13	ATF3	chr2:62732875-62733231	K562	blood:	n/a	n/a
14	ATF3	chr2:62733290-62733558	K562	blood:	n/a	n/a
15	BACH1	chr2:62710180-62710346	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr2:62692610-62693481	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:62695167-62695301	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:62732849-62733602	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:62702027-62702105	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr2:62703456-62703464	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr2:62701897-62702127	GM12878	blood:	n/a	n/a
22	BCL3	chr2:62732715-62733916	A549	lung:	n/a	n/a
23	BCL3	chr2:62732782-62733745	A549	lung:	n/a	n/a
24	BCLAF1	chr2:62732647-62733142	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:62695190-62695387	K562	blood:	n/a	n/a
26	BHLHE40	chr2:62732400-62733822	K562	blood:	n/a	chr2:62732965-62732981
27	BHLHE40	chr2:62696382-62696466	K562	blood:	n/a	n/a
28	BHLHE40	chr2:62732866-62733183	GM12878	blood:	n/a	chr2:62732965-62732981
29	BRCA1	chr2:62694802-62694810	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr2:62732916-62733298	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr2:62733481-62733625	GM12878	blood:	n/a	n/a
32	CBX3	chr2:62728490-62729230	K562	blood:	n/a	n/a
33	CBX3	chr2:62732770-62733748	K562	blood:	n/a	n/a
34	CCNT2	chr2:62732788-62733611	K562	blood:	n/a	n/a
35	CEBPB	chr2:62696361-62696556	K562	blood:	n/a	n/a
36	CEBPB	chr2:62712242-62712567	A549	lung:	n/a	chr2:62712385-62712402 chr2:62712388-62712399
37	CEBPB	chr2:62712304-62712504	K562	blood:	n/a	chr2:62712385-62712402 chr2:62712388-62712399
38	CEBPB	chr2:62694264-62695245	HepG2	liver:	n/a	chr2:62695214-62695225 chr2:62695057-62695068
39	CEBPB	chr2:62694976-62695182	HepG2	liver:	n/a	chr2:62695057-62695068
40	CEBPB	chr2:62728312-62728510	K562	blood:	n/a	n/a
41	CEBPB	chr2:62694267-62694740	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:62732970-62733051	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr2:62712225-62712556	HepG2	liver:	n/a	chr2:62712385-62712402 chr2:62712388-62712399
44	CEBPB	chr2:62723521-62723731	A549	lung:	n/a	n/a
45	CEBPB	chr2:62712241-62712566	Hela-S3	cervix:	n/a	chr2:62712385-62712402 chr2:62712388-62712399
46	CEBPB	chr2:62694384-62694607	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:62723476-62723771	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:62712245-62712559	IMR90	lung:	n/a	chr2:62712385-62712402 chr2:62712388-62712399
49	CEBPB	chr2:62732682-62733470	A549	lung:	n/a	n/a
50	CEBPB	chr2:62733371-62733419	H1-hESC	embryonic stem cell:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:62734870-62734920	ProgFib	skin:	n/a
2	chr2:62729106-62729156	NH-A	brain:	n/a
3	chr2:62734870-62734920	ProgFib	skin:	n/a
4	chr2:62729106-62729156	NH-A	brain:	n/a
5	chr2:62733576-62733626	NT2-D1	testis:	n/a
6	chr2:62714011-62714061	HIPEpiC	eye:	n/a
7	chr2:62714011-62714061	CMK	blood:	n/a
8	chr2:62733617-62733667	SK-N-SH_RA	brain:	n/a
9	chr2:62732450-62732500	NT2-D1	testis:	n/a
10	chr2:62736315-62736365	SK-N-SH_RA	brain:	n/a
11	chr2:62732450-62732500	HCF	heart:	n/a
12	chr2:62734870-62734920	HEEpiC	esophagus:	n/a
13	chr2:62733114-62733164	U87	brain:	n/a
14	chr2:62733114-62733164	GM12892	blood:	n/a
15	chr2:62734857-62734907	SAEC	small airway:	n/a
16	chr2:62733617-62733667	ovcar-3	ovarian:	n/a
17	chr2:62733114-62733164	Jurkat	blood:	n/a
18	chr2:62732450-62732500	MCF10A-Er-Src	breast:	n/a
19	chr2:62729106-62729156	BJ	skin:	n/a
20	chr2:62734857-62734907	ProgFib	skin:	n/a
21	chr2:62733485-62733535	AG09319	gingival:	n/a
22	chr2:62694068-62694118	NB4	blood:	n/a
23	chr2:62733617-62733667	HRCEpiC	kidney:	n/a
24	chr2:62732892-62732942	HRPEpiC	eye:	n/a
25	chr2:62734870-62734920	AG09319	gingival:	n/a
26	chr2:62729106-62729156	GM12891	blood:	n/a
27	chr2:62732892-62732942	K562	blood:	n/a
28	chr2:62734870-62734920	HCT-116	colon:	n/a
29	chr2:62732892-62732942	GM06990	blood:	n/a
30	chr2:62733485-62733535	HCPEpiC	choroid plexus:	n/a
31	chr2:62736315-62736365	GM12891	blood:	n/a
32	chr2:62729106-62729156	NHBE	bronchial:	n/a
33	chr2:62734857-62734907	PFSK-1	brain:	n/a
34	chr2:62734857-62734907	HEEpiC	esophagus:	n/a
35	chr2:62736315-62736365	AG09309	skin:	n/a
36	chr2:62734870-62734920	SKMC	muscle:	n/a
37	chr2:62694068-62694118	RPTEC	kidney:	n/a
38	chr2:62733617-62733667	Hepatocyte	liver:	n/a
39	chr2:62734870-62734920	MCF-7	breast:	n/a
40	chr2:62702472-62702522	HRPEpiC	eye:	n/a
41	chr2:62736315-62736365	GM12878	blood:	n/a
42	chr2:62736315-62736365	HEK293	kidney:	embryo
43	chr2:62702472-62702522	MCF-7	breast:	n/a
44	chr2:62734857-62734907	U87	brain:	n/a
45	chr2:62702472-62702522	HRE	kidney:	n/a
46	chr2:62732450-62732500	T-47D	breast:	n/a
47	chr2:62733576-62733626	U87	brain:	n/a
48	chr2:62733166-62733216	HMEC	breast:	n/a
49	chr2:62729106-62729156	HCM	heart:	n/a
50	chr2:62733617-62733667	HRE	kidney:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:62713307..62714054-chr2:62723005..62723908,2	MCF-7	breast:
2	chr2:62730535..62732862-chr2:62735147..62737485,2	K562	blood:
3	chr2:62724451..62726698-chr2:62729521..62731262,2	MCF-7	breast:
4	chr2:62690827..62693709-chr2:62697942..62699978,2	K562	blood:
5	chr2:62693761..62695980-chr2:62731518..62734032,2	K562	blood:
6	chr2:62731472..62734976-chr2:62932827..62936526,3	K562	blood:
7	chr2:62732196..62734647-chr2:62932204..62934327,2	K562	blood:
8	chr2:62732443..62734653-chr2:62900758..62903078,2	MCF-7	breast:
9	chr2:62730535..62732862-chr2:62735147..62737485,2	K562	blood:
10	chr2:62722458..62725305-chr2:62733715..62736301,2	MCF-7	breast:
11	chr2:62703410..62705239-chr2:62732311..62734145,2	MCF-7	breast:
12	chr2:62713307..62714054-chr2:62723005..62723908,2	MCF-7	breast:
13	chr2:62723131..62724977-chr2:62729168..62731291,2	K562	blood:
14	chr2:62706782..62709578-chr2:62731639..62733340,2	K562	blood:
15	chr2:62695267..62696888-chr2:62697506..62699070,2	K562	blood:
16	chr2:62690827..62693709-chr2:62697942..62699978,2	K562	blood:
17	chr2:62723131..62724977-chr2:62729168..62731291,2	K562	blood:
18	chr2:62735658..62737630-chr2:62932530..62934891,2	MCF-7	breast:
19	chr2:62718276..62720526-chr2:62727319..62729124,2	MCF-7	breast:
20	chr2:62720855..62722462-chr2:62729952..62731670,2	MCF-7	breast:
21	chr2:62720855..62722462-chr2:62729952..62731670,2	MCF-7	breast:
22	chr2:62707580..62709394-chr2:62711860..62714496,2	MCF-7	breast:
23	chr2:62704342..62706452-chr2:62754293..62757210,2	K562	blood:
24	chr2:62733287..62736036-chr2:62952497..62954456,3	MCF-7	breast:
25	chr2:62695278..62697363-chr2:62699071..62703066,3	MCF-7	breast:
26	chr2:62694347..62696888-chr2:62697503..62699006,2	K562	blood:
27	chr2:62732945..62733646-chr2:62932143..62933056,2	MCF-7	breast:
28	chr2:62695278..62697363-chr2:62699071..62703066,3	MCF-7	breast:
29	chr2:62724451..62726698-chr2:62729521..62731262,2	MCF-7	breast:
30	chr2:62693720..62695307-chr2:62932805..62934565,2	K562	blood:
31	chr2:62735980..62738470-chr2:62739827..62741870,2	K562	blood:
32	chr2:62721226..62723259-chr2:62730876..62733526,2	MCF-7	breast:
33	chr2:62707580..62709394-chr2:62711860..62714496,2	MCF-7	breast:
34	chr2:62706782..62709578-chr2:62731639..62733340,2	K562	blood:
35	chr2:62694347..62696888-chr2:62697503..62699006,2	K562	blood:
36	chr2:62695267..62696888-chr2:62697506..62699070,2	K562	blood:
37	chr2:62730719..62734296-chr2:62930912..62935708,9	MCF-7	breast:
38	chr2:62726106..62729574-chr2:62730789..62734406,4	MCF-7	breast:
39	chr2:62731742..62734497-chr2:62931519..62934102,3	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDPCP-9	chr2:62734680-62734958	NONHSAT071018
2	lnc-TMEM17-3	chr2:62705592-62705650	NONHSAT071016
3	lnc-TMEM17-3	chr2:62692511-62692862	NONHSAT071016
4	lnc-EHBP1-3	chr2:62718313-62718601	NONHSAT071017
5	lnc-TMEM17-3	chr2:62705592-62705690	l_1844_chr2:62668271-62712206_testes
6	lnc-TMEM17-3	chr2:62712041-62712204	NONHSAT071013
7	lnc-TMEM17-3	chr2:62691897-62692862	l_1844_chr2:62668271-62712206_testes
8	lnc-TMEM17-3	chr2:62709992-62710115	NONHSAT071016
9	lnc-TMEM17-3	chr2:62712041-62712204	NONHSAT071016
10	lnc-TMEM17-3	chr2:62692955-62693030	l_1844_chr2:62668271-62712206_testes
11	lnc-TMEM17-3	chr2:62709992-62710083	l_1844_chr2:62668271-62712206_testes
12	lnc-TMEM17-3	chr2:62712041-62712206	l_1844_chr2:62668271-62712206_testes
13	lnc-TMEM17-3	chr2:62694245-62694341	NONHSAT071016
14	lnc-TMEM17-3	chr2:62692955-62693030	NONHSAT071016

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TMEM17	hsa-miR-192-5p	chr2:62727816-62727837

Variant related genes	Relation type
RN7SL18P	TF binding region
TMEM17	TF binding region
ENSG00000233702	TF binding region
RN7SL18P	CpG island
TMEM17	CpG island
ENSG00000233702	CpG island
ENSG00000115504	chromatin interactions
ENSG00000241625	chromatin interactions
ENSG00000252436	chromatin interactions
ENSG00000233702	chromatin interactions
ENSG00000186889	chromatin interactions

Extended variants
information (count: 1753 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1753 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537496297	chr2:62691273-62691274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139490368	chr2:62691275-62691276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567601343	chr2:62691281-62691282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372725142	chr2:62691330-62691331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149827174	chr2:62691331-62691332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571541187	chr2:62691371-62691372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538824522	chr2:62691394-62691395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556684467	chr2:62691397-62691398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190509781	chr2:62691408-62691409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115158161	chr2:62691410-62691411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183806588	chr2:62691416-62691417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78477478	chr2:62691435-62691436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533958077	chr2:62691440-62691441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540568422	chr2:62691484-62691485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554138189	chr2:62691505-62691506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372323515	chr2:62691525-62691526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116117326	chr2:62691533-62691534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145794506	chr2:62691558-62691559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544412946	chr2:62691562-62691563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35848735	chr2:62691598-62691599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562350464	chr2:62691624-62691625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370037010	chr2:62691643-62691644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78282363	chr2:62691644-62691645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555743329	chr2:62691662-62691663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549425813	chr2:62691663-62691664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369047719	chr2:62691717-62691718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140727744	chr2:62691763-62691764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187897649	chr2:62691820-62691821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546916988	chr2:62691828-62691829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191614626	chr2:62691843-62691844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7581180	chr2:62691850-62691851	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557142097	chr2:62691890-62691891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182538909	chr2:62691903-62691904	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs535980322	chr2:62691922-62691923	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs75104627	chr2:62691949-62691950	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs368567517	chr2:62691951-62691952	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs564233639	chr2:62691957-62691958	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs116135962	chr2:62691968-62691969	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs371153714	chr2:62692013-62692014	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs540231885	chr2:62692055-62692056	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs558936196	chr2:62692161-62692162	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs186496008	chr2:62692200-62692201	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs544468939	chr2:62692242-62692243	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs562561150	chr2:62692250-62692251	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs529862307	chr2:62692260-62692261	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs572180783	chr2:62692274-62692275	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs113095852	chr2:62692304-62692305	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs74904598	chr2:62692305-62692306	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs76946030	chr2:62692318-62692319	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs374090052	chr2:62692327-62692328	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD

Chromatin state (count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:62684800-62693600	Weak transcription	Right Atrium	heart
2	chr2:62684800-62700800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr2:62685000-62694600	Enhancers	HepG2	liver
4	chr2:62685000-62696600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr2:62685600-62693400	Weak transcription	Ovary	ovary
6	chr2:62686200-62693400	Weak transcription	Adipose Nuclei	Adipose
7	chr2:62686200-62699000	Weak transcription	HSMMtube	muscle
8	chr2:62686600-62692600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:62687400-62693600	Weak transcription	Fetal Brain Female	brain
10	chr2:62687600-62693400	Weak transcription	Fetal Brain Male	brain
11	chr2:62688000-62693200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:62688200-62692800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:62688200-62693000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:62688200-62693200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:62689200-62691400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:62689200-62693400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:62689200-62694400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:62689200-62694400	Weak transcription	NHEK	skin
19	chr2:62689400-62693400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr2:62689400-62693400	Weak transcription	Colon Smooth Muscle	Colon
21	chr2:62689400-62693400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr2:62689400-62693400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr2:62689400-62694400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr2:62689400-62694600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr2:62689400-62694600	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr2:62689600-62691600	Enhancers	Liver	Liver
27	chr2:62689600-62693000	Weak transcription	Fetal Muscle Leg	muscle
28	chr2:62689600-62693000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr2:62689600-62693400	Weak transcription	Esophagus	oesophagus
30	chr2:62689600-62693600	Weak transcription	NHDF-Ad	bronchial
31	chr2:62689600-62693600	Weak transcription	NHLF	lung
32	chr2:62689600-62697000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr2:62689800-62691600	Weak transcription	Osteobl	bone
34	chr2:62689800-62693600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr2:62690000-62693600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr2:62690200-62691400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:62690200-62693000	Weak transcription	A549	lung
38	chr2:62690400-62692800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr2:62690400-62694600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr2:62690400-62700600	Weak transcription	Fetal Intestine Large	intestine
41	chr2:62690600-62691800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr2:62690800-62691600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:62691000-62693400	Weak transcription	Placenta	Placenta
44	chr2:62691000-62693800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr2:62691000-62695400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr2:62691200-62691600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:62691200-62691600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:62691200-62691800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:62691200-62691800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr2:62691200-62692000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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