Variant report

Variant	nsv583497
Chromosome Location	chr2:160963603-161079435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1899)
CpG islands
(count:488)
Chromatin interactive
region (count:135)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1899 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:161078278-161078457	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:160966482-160966795	HepG2	liver:	n/a	n/a
3	ATF2	chr2:160968650-160969144	GM12878	blood:	n/a	n/a
4	ATF2	chr2:161066976-161067513	GM12878	blood:	n/a	n/a
5	ATF3	chr2:161061841-161062531	A549	lung:	n/a	n/a
6	BATF	chr2:160968776-160969110	GM12878	blood:	n/a	n/a
7	BATF	chr2:161064614-161064922	GM12878	blood:	n/a	chr2:161064771-161064782 chr2:161064772-161064782
8	BATF	chr2:160968686-160969071	GM12878	blood:	n/a	n/a
9	BATF	chr2:161067060-161067418	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:160968700-160969078	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:161058766-161058948	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:161066148-161066422	GM12878	blood:	n/a	chr2:161066272-161066281
13	BCL11A	chr2:160968807-160969070	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:161066976-161067389	GM12878	blood:	n/a	n/a
15	BCL3	chr2:161061875-161062556	A549	lung:	n/a	n/a
16	BCL3	chr2:161064437-161065397	A549	lung:	n/a	chr2:161064444-161064453
17	BCL3	chr2:161064376-161065131	A549	lung:	n/a	chr2:161064444-161064453
18	BCL3	chr2:161061641-161062542	A549	lung:	n/a	n/a
19	BCL3	chr2:161065862-161066583	A549	lung:	n/a	chr2:161066272-161066281
20	BCLAF1	chr2:161067008-161067602	GM12878	blood:	n/a	chr2:161067438-161067447 chr2:161067439-161067448
21	BCLAF1	chr2:161067091-161067467	GM12878	blood:	n/a	chr2:161067438-161067447 chr2:161067439-161067448
22	BCLAF1	chr2:161058650-161059009	GM12878	blood:	n/a	n/a
23	BHLHE40	chr2:161064675-161065152	HepG2	liver:	n/a	n/a
24	BHLHE40	chr2:160968635-160969253	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:161067105-161067484	K562	blood:	n/a	n/a
26	BHLHE40	chr2:161058744-161059006	GM12878	blood:	n/a	n/a
27	BHLHE40	chr2:161066938-161067481	GM12878	blood:	n/a	n/a
28	BHLHE40	chr2:161059690-161059830	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:160966521-160966814	GM12878	blood:	n/a	n/a
30	BHLHE40	chr2:161064536-161065131	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:161079407-161079804	HepG2	liver:	n/a	n/a
32	BHLHE40	chr2:161063634-161063941	GM12878	blood:	n/a	n/a
33	BHLHE40	chr2:161066225-161066550	GM12878	blood:	n/a	n/a
34	BRCA1	chr2:161076854-161077240	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr2:161061792-161062467	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr2:161061795-161062661	HCT-116	colon:	n/a	n/a
37	CBX3	chr2:161064451-161065155	HCT-116	colon:	n/a	chr2:161064561-161064572
38	CBX3	chr2:161061813-161062732	HCT-116	colon:	n/a	n/a
39	CEBPB	chr2:161065894-161066579	A549	lung:	n/a	n/a
40	CEBPB	chr2:161014455-161014697	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:161013175-161013573	IMR90	lung:	n/a	n/a
42	CEBPB	chr2:160998326-160998838	MCF-7	breast:	n/a	n/a
43	CEBPB	chr2:160965963-160966725	A549	lung:	n/a	chr2:160966306-160966317
44	CEBPB	chr2:161064293-161064428	K562	blood:	n/a	n/a
45	CEBPB	chr2:161065979-161066459	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:161028096-161028400	HepG2	liver:	n/a	chr2:161028232-161028243
47	CEBPB	chr2:161028117-161028337	IMR90	lung:	n/a	chr2:161028232-161028243
48	CEBPB	chr2:160998351-160998833	MCF-7	breast:	n/a	n/a
49	CEBPB	chr2:161063682-161065449	A549	lung:	n/a	chr2:161064568-161064576
50	CEBPB	chr2:161071151-161071513	Hela-S3	cervix:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:161061541-161061591	LNCaP	prostate:	n/a
2	chr2:161052031-161052081	SKMC	muscle:	n/a
3	chr2:161056520-161056570	HAEpiC	amniotic membrane:	n/a
4	chr2:161056639-161056689	SAEC	small airway:	n/a
5	chr2:161052031-161052081	H1-hESC	embryonic stem cell:	embryo
6	chr2:161056639-161056689	HCPEpiC	choroid plexus:	n/a
7	chr2:161077747-161077797	K562	blood:	n/a
8	chr2:161061541-161061591	IMR90	lung:	fetal
9	chr2:161070749-161070799	GM19239	blood:	n/a
10	chr2:161052031-161052081	GM06990	blood:	n/a
11	chr2:161057625-161057675	HEK293	kidney:	embryo
12	chr2:161077747-161077797	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:161070749-161070799	NH-A	brain:	n/a
14	chr2:161070749-161070799	A549	lung:	n/a
15	chr2:161077747-161077797	NHBE	bronchial:	n/a
16	chr2:161052031-161052081	HL-60	blood:	n/a
17	chr2:161056639-161056689	A549	lung:	n/a
18	chr2:161056639-161056689	T-47D	breast:	n/a
19	chr2:161056639-161056689	HIPEpiC	eye:	n/a
20	chr2:161056600-161056650	SAEC	small airway:	n/a
21	chr2:161056600-161056650	AG09319	gingival:	n/a
22	chr2:161077747-161077797	HUVEC	blood vessel:	n/a
23	chr2:161056600-161056650	PFSK-1	brain:	n/a
24	chr2:161061541-161061591	HCPEpiC	choroid plexus:	n/a
25	chr2:161056520-161056570	PANC-1	pancreas:	n/a
26	chr2:161057625-161057675	NH-A	brain:	n/a
27	chr2:161056520-161056570	HEK293	kidney:	embryo
28	chr2:161056600-161056650	PrEC	prostate:	n/a
29	chr2:161061541-161061591	BE2_C	brain:	n/a
30	chr2:161056639-161056689	H1-hESC	embryonic stem cell:	embryo
31	chr2:161057625-161057675	HIPEpiC	eye:	n/a
32	chr2:161077747-161077797	HCT-116	colon:	n/a
33	chr2:161061541-161061591	HCM	heart:	n/a
34	chr2:161056639-161056689	RPTEC	kidney:	n/a
35	chr2:161056600-161056650	HNPCEpiC	eye:	n/a
36	chr2:161061541-161061591	HRE	kidney:	n/a
37	chr2:161056600-161056650	SK-N-SH	brain:	n/a
38	chr2:161077747-161077797	Hela-S3	cervix:	n/a
39	chr2:161057625-161057675	HCM	heart:	n/a
40	chr2:161077747-161077797	AoSMC	blood vessel:	n/a
41	chr2:161056520-161056570	NB4	blood:	n/a
42	chr2:161056600-161056650	HL-60	blood:	n/a
43	chr2:161061541-161061591	AG09309	skin:	n/a
44	chr2:161077747-161077797	NB4	blood:	n/a
45	chr2:161056520-161056570	HUVEC	blood vessel:	n/a
46	chr2:161070749-161070799	IMR90	lung:	fetal
47	chr2:161061541-161061591	HL-60	blood:	n/a
48	chr2:161056639-161056689	LNCaP	prostate:	n/a
49	chr2:161070749-161070799	SAEC	small airway:	n/a
50	chr2:161057625-161057675	BJ	skin:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:161078259..161081272-chr2:162015339..162019346,4	MCF-7	breast:
2	chr2:161047148..161049457-chr2:161049468..161051501,2	MCF-7	breast:
3	chr2:160997062..160999873-chr2:161011563..161014295,2	MCF-7	breast:
4	chr2:161047148..161049457-chr2:161049468..161051501,2	MCF-7	breast:
5	chr2:161034766..161037717-chr2:161047419..161049441,2	MCF-7	breast:
6	chr2:161020904..161022574-chr2:161030651..161033294,2	MCF-7	breast:
7	chr2:161011918..161014903-chr2:161016994..161018899,2	K562	blood:
8	chr2:161011673..161014390-chr2:161015333..161017860,2	MCF-7	breast:
9	chr2:161030988..161033142-chr2:161065099..161067240,2	MCF-7	breast:
10	chr2:161015690..161017268-chr2:161021219..161023930,2	MCF-7	breast:
11	chr2:161000991..161002542-chr2:161026874..161029211,2	MCF-7	breast:
12	chr2:161023086..161025481-chr2:161028463..161031210,2	MCF-7	breast:
13	chr2:160992962..160997280-chr2:160998915..161002711,4	K562	blood:
14	chr2:160993718..160995794-chr2:160997568..160999439,2	MCF-7	breast:
15	chr2:161012780..161016073-chr2:161064751..161067692,4	MCF-7	breast:
16	chr2:161011444..161016530-chr2:161074862..161081219,9	MCF-7	breast:
17	chr2:161022710..161025666-chr2:161026068..161028687,2	MCF-7	breast:
18	chr2:161029423..161031683-chr2:161033296..161035758,2	MCF-7	breast:
19	chr2:161075979..161078708-chr2:161349320..161350838,2	MCF-7	breast:
20	chr2:160969923..160971430-chr2:161063576..161065947,2	MCF-7	breast:
21	chr2:161034766..161037717-chr2:161047419..161049441,2	MCF-7	breast:
22	chr2:160982529..160984640-chr2:161078156..161079933,2	MCF-7	breast:
23	chr2:161025898..161028586-chr2:161060919..161062605,2	MCF-7	breast:
24	chr2:161000112..161002842-chr2:161027169..161029887,2	MCF-7	breast:
25	chr2:160997062..160999873-chr2:161011563..161014295,2	MCF-7	breast:
26	chr2:160978525..160981101-chr2:160983731..160985356,2	MCF-7	breast:
27	chr2:160956526..160958780-chr2:161077577..161080506,2	MCF-7	breast:
28	chr2:161009313..161012082-chr2:161014084..161016057,3	MCF-7	breast:
29	chr2:160981983..160984926-chr2:160986223..160988366,2	K562	blood:
30	chr2:160981270..160984730-chr2:160985198..160987380,3	MCF-7	breast:
31	chr2:160964286..160967312-chr2:161082194..161085973,4	MCF-7	breast:
32	chr2:160981270..160984730-chr2:160985198..160987380,3	MCF-7	breast:
33	chr2:160978525..160981101-chr2:160983731..160985356,2	MCF-7	breast:
34	chr2:161023086..161025221-chr2:161061851..161065492,3	MCF-7	breast:
35	chr2:161023086..161025481-chr2:161028463..161031210,2	MCF-7	breast:
36	chr2:160966552..160967071-chr2:161066902..161067530,2	MCF-7	breast:
37	chr2:160992962..160995573-chr2:161000331..161001986,2	K562	blood:
38	chr2:160981983..160984926-chr2:160986223..160988366,2	K562	blood:
39	chr2:161000991..161002542-chr2:161026874..161029211,2	MCF-7	breast:
40	chr2:161022219..161025044-chr2:161064503..161066413,2	MCF-7	breast:
41	chr2:160750717..160753451-chr2:160965407..160967520,2	MCF-7	breast:
42	chr2:161012780..161016073-chr2:161064751..161067692,4	MCF-7	breast:
43	chr2:161044639..161046175-chr2:161046319..161048023,2	MCF-7	breast:
44	chr2:161021190..161023892-chr2:161082656..161085932,3	MCF-7	breast:
45	chr2:160977849..160980752-chr2:161063430..161065626,2	MCF-7	breast:
46	chr2:161014948..161017596-chr2:161095953..161098533,2	MCF-7	breast:
47	chr2:161000112..161002842-chr2:161027169..161029887,2	MCF-7	breast:
48	chr2:160966312..160970362-chr2:161075037..161076917,3	MCF-7	breast:
49	chr2:161055546..161057475-chr2:161125136..161129505,3	MCF-7	breast:
50	chr2:160982529..160984640-chr2:161078156..161079933,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBMS1-3	chr2:161057284-161057728	NONHSAT075132

No data

Variant related genes	Relation type
ITGB6	TF binding region
ITGB6	CpG island
ENSG00000202077	chromatin interactions
ENSG00000153246	chromatin interactions
ENSG00000224467	chromatin interactions
ENSG00000136560	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000153250	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000115221	chromatin interactions
ENSG00000005483	chromatin interactions

Extended variants
information (count: 4658 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:4658 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10497213	chr2:160963603-160963604	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559277468	chr2:160963638-160963639	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138963669	chr2:160963694-160963695	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs60843445	chr2:160963700-160963701	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182473852	chr2:160963717-160963718	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186750444	chr2:160963777-160963778	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112490733	chr2:160963786-160963787	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531062144	chr2:160963804-160963805	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552801165	chr2:160963848-160963849	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374478726	chr2:160963872-160963873	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74399321	chr2:160963886-160963887	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546953738	chr2:160963908-160963909	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4450558	chr2:160963958-160963959	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35607753	chr2:160964054-160964055	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71422292	chr2:160964057-160964058	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114109844	chr2:160964058-160964059	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201566540	chr2:160964059-160964060	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535091514	chr2:160964075-160964076	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556946634	chr2:160964080-160964081	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6724949	chr2:160964100-160964101	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs367594080	chr2:160964120-160964121	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557490065	chr2:160964131-160964132	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11888415	chr2:160964162-160964163	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs150867142	chr2:160964191-160964192	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540109604	chr2:160964212-160964213	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199651918	chr2:160964213-160964214	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370595727	chr2:160964223-160964224	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374327754	chr2:160964258-160964259	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146397669	chr2:160964288-160964289	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573911717	chr2:160964314-160964315	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367865998	chr2:160964323-160964324	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs267598939	chr2:160964325-160964326	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372646338	chr2:160964327-160964328	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377135299	chr2:160964339-160964340	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369122182	chr2:160964350-160964351	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541836085	chr2:160964407-160964408	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13010138	chr2:160964457-160964458	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs572058188	chr2:160964520-160964521	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139742983	chr2:160964527-160964528	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546325626	chr2:160964534-160964535	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150055690	chr2:160964633-160964634	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548805493	chr2:160964645-160964646	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570558133	chr2:160964665-160964666	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547279266	chr2:160964699-160964700	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10497212	chr2:160964700-160964701	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs71408112	chr2:160964726-160964727	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57363305	chr2:160964755-160964756	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78111276	chr2:160964765-160964766	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59209381	chr2:160964766-160964767	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192405130	chr2:160964824-160964825	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
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
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
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	18414403	CNVD
Epilepsy	21204806	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:160950800-160967000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:160953200-160970800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:160954600-160970800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:160954600-160993000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr2:160954800-160963800	Weak transcription	Fetal Intestine Large	intestine
6	chr2:160954800-160966200	Weak transcription	Fetal Intestine Small	intestine
7	chr2:160955400-160965000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:160955800-160968800	Weak transcription	Fetal Muscle Trunk	muscle
9	chr2:160956200-160965600	Strong transcription	HMEC	breast
10	chr2:160957000-160970200	Weak transcription	Pancreas	Pancrea
11	chr2:160957400-160981200	Weak transcription	Lung	lung
12	chr2:160958400-160965200	Strong transcription	NHEK	skin
13	chr2:160959200-160963800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr2:160959200-161004200	Weak transcription	Gastric	stomach
15	chr2:160959400-160985200	Weak transcription	Esophagus	oesophagus
16	chr2:160959400-161032800	Weak transcription	Psoas Muscle	Psoas
17	chr2:160959800-160965800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr2:160960000-160966400	Weak transcription	HSMMtube	muscle
19	chr2:160960400-160965600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:160960800-160964600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr2:160961000-160965600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr2:160962000-160966200	Strong transcription	HSMM	muscle
23	chr2:160962400-160963800	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr2:160962400-160970800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr2:160962800-160971000	Strong transcription	Placenta Amnion	Placenta Amnion
26	chr2:160963800-160964400	Strong transcription	Fetal Intestine Large	intestine
27	chr2:160963800-160964400	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr2:160963800-160969200	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr2:160964000-160964200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:160964200-160993600	Weak transcription	Fetal Muscle Leg	muscle
31	chr2:160964400-160965800	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr2:160964400-160967000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:160964400-160993600	Weak transcription	Fetal Intestine Large	intestine
34	chr2:160964600-160965400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:160964800-160966200	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr2:160964800-160970800	Weak transcription	Stomach Mucosa	stomach
37	chr2:160965000-160966400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr2:160965000-160968200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:160965200-160965600	Weak transcription	NHEK	skin
40	chr2:160965200-160968000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:160965400-160966400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:160965400-160966600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:160965600-160966400	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr2:160965600-160967600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr2:160965600-160968000	Genic enhancers	NHEK	skin
46	chr2:160965600-160969200	Genic enhancers	HMEC	breast
47	chr2:160965800-160966400	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr2:160965800-160967200	Enhancers	Muscle Satellite Cultured Cells	--
49	chr2:160965800-160969600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr2:160966000-160968000	Enhancers	A549	lung

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