Variant report

Variant	nsv875381
Chromosome Location	chr2:169686559-169749841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:921)
CpG islands
(count:794)
Chromatin interactive
region (count:48)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:921 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:169708023-169709049	K562	blood:	n/a	n/a
2	ARID3A	chr2:169747677-169747689	K562	blood:	n/a	n/a
3	ARID3A	chr2:169746801-169747329	K562	blood:	n/a	n/a
4	ARID3A	chr2:169706158-169706387	HepG2	liver:	n/a	n/a
5	ATF1	chr2:169708240-169708848	K562	blood:	n/a	n/a
6	ATF3	chr2:169708197-169708764	K562	blood:	n/a	n/a
7	ATF3	chr2:169708305-169708569	K562	blood:	n/a	n/a
8	BACH1	chr2:169708355-169708555	K562	blood:	n/a	n/a
9	BACH1	chr2:169746453-169746544	K562	blood:	n/a	n/a
10	BCLAF1	chr2:169708103-169708891	K562	blood:	n/a	chr2:169708860-169708869
11	BCLAF1	chr2:169746705-169747215	GM12878	blood:	n/a	chr2:169746908-169746921
12	BHLHE40	chr2:169709621-169709807	K562	blood:	n/a	n/a
13	BHLHE40	chr2:169711340-169711381	K562	blood:	n/a	n/a
14	BHLHE40	chr2:169746757-169747257	K562	blood:	n/a	n/a
15	BHLHE40	chr2:169706194-169706403	HepG2	liver:	n/a	n/a
16	BHLHE40	chr2:169708173-169708867	K562	blood:	n/a	n/a
17	BRCA1	chr2:169746805-169747218	HepG2	liver:	n/a	n/a
18	BRCA1	chr2:169746849-169747201	GM12878	blood:	n/a	n/a
19	BRCA1	chr2:169746694-169747342	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr2:169746794-169747205	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr2:169708046-169708957	K562	blood:	n/a	n/a
22	CBX3	chr2:169708223-169708820	K562	blood:	n/a	n/a
23	CBX3	chr2:169746085-169747364	K562	blood:	n/a	chr2:169746470-169746481
24	CCNT2	chr2:169746745-169747073	K562	blood:	n/a	n/a
25	CCNT2	chr2:169735214-169735403	K562	blood:	n/a	n/a
26	CCNT2	chr2:169708156-169708954	K562	blood:	n/a	n/a
27	CEBPB	chr2:169701032-169701084	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:169708185-169708753	K562	blood:	n/a	n/a
29	CEBPB	chr2:169746600-169747089	K562	blood:	n/a	n/a
30	CEBPB	chr2:169746602-169747228	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:169688250-169688450	HepG2	liver:	n/a	chr2:169688320-169688331 chr2:169688338-169688349
32	CEBPB	chr2:169708113-169708821	K562	blood:	n/a	n/a
33	CEBPB	chr2:169746672-169746958	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:169746561-169747327	K562	blood:	n/a	n/a
35	CEBPD	chr2:169708115-169708967	K562	blood:	n/a	n/a
36	CEBPD	chr2:169746599-169746984	HepG2	liver:	n/a	n/a
37	CEBPD	chr2:169746495-169747268	K562	blood:	n/a	n/a
38	CEBPD	chr2:169708130-169709012	K562	blood:	n/a	n/a
39	CHD2	chr2:169709101-169709301	K562	blood:	n/a	n/a
40	CHD2	chr2:169708213-169708748	K562	blood:	n/a	n/a
41	CHD2	chr2:169746583-169747298	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr2:169746719-169747287	HepG2	liver:	n/a	n/a
43	CHD2	chr2:169746497-169747318	GM12878	blood:	n/a	n/a
44	CHD2	chr2:169746467-169747257	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr2:169746529-169747449	K562	blood:	n/a	n/a
46	CREB1	chr2:169746730-169747143	A549	lung:	n/a	n/a
47	CREB1	chr2:169746628-169747233	GM12878	blood:	n/a	n/a
48	CREB1	chr2:169746616-169747363	HepG2	liver:	n/a	n/a
49	CREB1	chr2:169708017-169709384	K562	blood:	n/a	n/a
50	CTCF	chr2:169706200-169706350	HAc	cerebellar:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:169744361-169744411	GM12892	blood:	n/a
2	chr2:169744361-169744411	GM12892	blood:	n/a
3	chr2:169747004-169747054	SK-N-MC	brain:	n/a
4	chr2:169744361-169744411	BJ	skin:	n/a
5	chr2:169746965-169747015	AG09319	gingival:	n/a
6	chr2:169747227-169747277	NT2-D1	testis:	n/a
7	chr2:169747050-169747100	PANC-1	pancreas:	n/a
8	chr2:169744361-169744411	NT2-D1	testis:	n/a
9	chr2:169747119-169747169	CMK	blood:	n/a
10	chr2:169746895-169746945	NB4	blood:	n/a
11	chr2:169746965-169747015	T-47D	breast:	n/a
12	chr2:169714050-169714100	CMK	blood:	n/a
13	chr2:169746671-169746721	HCM	heart:	n/a
14	chr2:169746671-169746721	Hela-S3	cervix:	n/a
15	chr2:169747178-169747228	AG04450	lung:	fetal
16	chr2:169746998-169747048	GM12891	blood:	n/a
17	chr2:169744361-169744411	HIPEpiC	eye:	n/a
18	chr2:169747227-169747277	IMR90	lung:	fetal
19	chr2:169746965-169747015	PANC-1	pancreas:	n/a
20	chr2:169746895-169746945	RPTEC	kidney:	n/a
21	chr2:169746965-169747015	AG09309	skin:	n/a
22	chr2:169746965-169747015	Hela-S3	cervix:	n/a
23	chr2:169747004-169747054	NHDF-neo	bronchial:	n/a
24	chr2:169747004-169747054	GM12891	blood:	n/a
25	chr2:169714050-169714100	HCF	heart:	n/a
26	chr2:169746671-169746721	HCF	heart:	n/a
27	chr2:169746958-169747008	T-47D	breast:	n/a
28	chr2:169746998-169747048	CMK	blood:	n/a
29	chr2:169744361-169744411	GM12891	blood:	n/a
30	chr2:169747050-169747100	HCM	heart:	n/a
31	chr2:169747004-169747054	NT2-D1	testis:	n/a
32	chr2:169746958-169747008	HAEpiC	amniotic membrane:	n/a
33	chr2:169747178-169747228	SK-N-SH	brain:	n/a
34	chr2:169747227-169747277	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:169747227-169747277	K562	blood:	n/a
36	chr2:169746895-169746945	BE2_C	brain:	n/a
37	chr2:169747004-169747054	HCPEpiC	choroid plexus:	n/a
38	chr2:169746998-169747048	PrEC	prostate:	n/a
39	chr2:169746998-169747048	HCT-116	colon:	n/a
40	chr2:169714050-169714100	NHBE	bronchial:	n/a
41	chr2:169746720-169746770	ECC-1	luminal epithelium:	n/a
42	chr2:169746895-169746945	HCF	heart:	n/a
43	chr2:169746895-169746945	HEEpiC	esophagus:	n/a
44	chr2:169746720-169746770	CMK	blood:	n/a
45	chr2:169714050-169714100	SK-N-MC	brain:	n/a
46	chr2:169747050-169747100	AG09309	skin:	n/a
47	chr2:169747119-169747169	Jurkat	blood:	n/a
48	chr2:169747119-169747169	HepG2	liver:	n/a
49	chr2:169747227-169747277	U87	brain:	n/a
50	chr2:169746895-169746945	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:169685233..169688150-chr2:169693345..169695299,2	K562	blood:
2	chr2:169736562..169739615-chr2:169739927..169743457,5	K562	blood:
3	chr2:169728195..169733629-chr2:169741403..169748359,8	K562	blood:
4	chr2:169743474..169745505-chr2:169745561..169748258,2	K562	blood:
5	chr2:169712836..169714967-chr2:169721509..169723147,2	K562	blood:
6	chr2:169712682..169714336-chr2:169721625..169723147,2	K562	blood:
7	chr12:54718655..54719474-chr2:169720398..169720917,2	Hela-S3	cervix:
8	chr1:28831833..28832817-chr2:169720397..169720916,2	Hela-S3	cervix:
9	chr2:169701436..169703096-chr2:169703453..169705070,2	K562	blood:
10	chr2:169702428..169704516-chr2:169706998..169708601,2	K562	blood:
11	chr2:169690889..169693435-chr2:169695590..169697222,2	K562	blood:
12	chr2:169678781..169680698-chr2:169684813..169687488,2	K562	blood:
13	chr2:169733481..169736243-chr2:169763377..169765605,2	K562	blood:
14	chr2:169686945..169689727-chr2:169700154..169704422,5	K562	blood:
15	chr2:169631455..169632974-chr2:169701424..169703955,2	K562	blood:
16	chr2:169686945..169689727-chr2:169700154..169704422,5	K562	blood:
17	chr2:169747099..169750807-chr2:169751423..169754919,4	K562	blood:
18	chr2:169740008..169742410-chr20:3801025..3803112,2	K562	blood:
19	chr2:169735885..169738323-chr2:169767715..169770699,2	K562	blood:
20	chr2:169685233..169691832-chr2:169692007..169697159,7	K562	blood:
21	chr2:169736562..169739615-chr2:169739927..169743457,5	K562	blood:
22	chr2:169733180..169734791-chr2:169738462..169740668,2	K562	blood:
23	chr2:169700277..169703960-chr2:169704282..169708601,6	K562	blood:
24	chr2:169712682..169714336-chr2:169721625..169723147,2	K562	blood:
25	chr2:169685233..169691832-chr2:169692007..169697159,7	K562	blood:
26	chr2:169690889..169693435-chr2:169695590..169697222,2	K562	blood:
27	chr2:169666022..169668624-chr2:169702701..169704508,2	K562	blood:
28	chr2:169659171..169661687-chr2:169702085..169706270,3	K562	blood:
29	chr2:169700277..169703960-chr2:169704282..169708601,6	K562	blood:
30	chr2:169688270..169689994-chr2:169692260..169695194,2	MCF-7	breast:
31	chr2:169682202..169684023-chr2:169687028..169690817,4	K562	blood:
32	chr2:169629254..169632077-chr2:169708619..169710261,2	K562	blood:
33	chr2:169708518..169710215-chr2:169719291..169720993,2	K562	blood:
34	chr2:169697186..169698845-chr2:169698935..169700941,2	K562	blood:
35	chr2:169712836..169714967-chr2:169721509..169723147,2	K562	blood:
36	chr2:169702428..169704516-chr2:169706998..169708601,2	K562	blood:
37	chr2:169741332..169743279-chr2:169744791..169746494,2	K562	blood:
38	chr2:169653689..169656123-chr2:169689883..169693287,3	K562	blood:
39	chr2:169708518..169710215-chr2:169719291..169720993,2	K562	blood:
40	chr2:169688270..169689994-chr2:169692260..169695194,2	MCF-7	breast:
41	chr2:169710784..169714021-chr2:169716907..169719872,4	K562	blood:
42	chr2:169688344..169690142-chr2:169691245..169693238,2	K562	blood:
43	chr2:169701436..169703096-chr2:169703453..169705070,2	K562	blood:
44	chr2:169708194..169710093-chr2:169710266..169712297,2	K562	blood:
45	chr2:169685233..169688150-chr2:169693345..169695299,2	K562	blood:
46	chr2:169688344..169690142-chr2:169691245..169693238,2	K562	blood:
47	chr2:169695173..169698676-chr2:169698742..169702914,7	K562	blood:
48	chr2:169733180..169734791-chr2:169738462..169740668,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCB11-1	chr2:169702753-169703344	NONHSAT075340

No data

Variant related genes	Relation type
NOSTRIN	TF binding region
SPC25	TF binding region
NOSTRIN	CpG island
SPC25	CpG island
ENSG00000180198	chromatin interactions
ENSG00000125843	chromatin interactions
ENSG00000111481	chromatin interactions
ENSG00000152253	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000163072	chromatin interactions

Extended variants
information (count: 2645 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2645 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs487756	chr2:169686559-169686560	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372494457	chr2:169686618-169686619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184836372	chr2:169686620-169686621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376351435	chr2:169686646-169686647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140236634	chr2:169686658-169686659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559152023	chr2:169686682-169686683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575831807	chr2:169686707-169686708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375465210	chr2:169686738-169686739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544362101	chr2:169686752-169686753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564110021	chr2:169686779-169686780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528170940	chr2:169686782-169686783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533178629	chr2:169686793-169686794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376450347	chr2:169686803-169686804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560438450	chr2:169686830-169686831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71430648	chr2:169686836-169686837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542450593	chr2:169686838-169686839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541415377	chr2:169686864-169686865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188977496	chr2:169686907-169686908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548308350	chr2:169686992-169686993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548570203	chr2:169687022-169687023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144028436	chr2:169687031-169687032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35805236	chr2:169687049-169687050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531318567	chr2:169687057-169687058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551484738	chr2:169687067-169687068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570956018	chr2:169687071-169687072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370966644	chr2:169687081-169687082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375265162	chr2:169687163-169687164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368268340	chr2:169687191-169687192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140796206	chr2:169687198-169687199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75920387	chr2:169687211-169687212	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535821432	chr2:169687288-169687289	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs495074	chr2:169687341-169687342	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs495135	chr2:169687359-169687360	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs544356946	chr2:169687391-169687392	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558278069	chr2:169687415-169687416	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150450833	chr2:169687419-169687420	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540428160	chr2:169687510-169687511	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559966128	chr2:169687541-169687542	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192976883	chr2:169687679-169687680	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs519599	chr2:169687680-169687681	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562124778	chr2:169687686-169687687	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564927332	chr2:169687757-169687758	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551182202	chr2:169687772-169687773	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571330880	chr2:169687801-169687802	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533318362	chr2:169687891-169687892	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375126825	chr2:169687938-169687939	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567136077	chr2:169687940-169687941	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536141711	chr2:169688007-169688008	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs556122748	chr2:169688011-169688012	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs200260642	chr2:169688021-169688022	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	18414403	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Sudden cardiac death	19188705	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169660000-169688200	Weak transcription	Placenta	Placenta
2	chr2:169670000-169698000	Weak transcription	Stomach Mucosa	stomach
3	chr2:169670200-169690200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr2:169670600-169690800	Weak transcription	Fetal Stomach	stomach
5	chr2:169673400-169687600	Weak transcription	Right Ventricle	heart
6	chr2:169673400-169691600	Weak transcription	Colonic Mucosa	Colon
7	chr2:169673400-169692200	Weak transcription	Gastric	stomach
8	chr2:169676400-169687200	Weak transcription	Adipose Nuclei	Adipose
9	chr2:169676600-169687400	Weak transcription	Fetal Muscle Leg	muscle
10	chr2:169676600-169704800	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr2:169676600-169709600	Weak transcription	Fetal Muscle Trunk	muscle
12	chr2:169682000-169693600	Strong transcription	Rectal Mucosa Donor 31	rectum
13	chr2:169682200-169695000	Weak transcription	Small Intestine	intestine
14	chr2:169683400-169717600	Weak transcription	Ovary	ovary
15	chr2:169684000-169687600	Weak transcription	Lung	lung
16	chr2:169684200-169690200	Weak transcription	Pancreas	Pancrea
17	chr2:169685200-169689000	Strong transcription	Fetal Intestine Large	intestine
18	chr2:169685600-169694200	Strong transcription	Duodenum Mucosa	Duodenum
19	chr2:169685800-169689000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr2:169686000-169691200	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr2:169686000-169693600	Strong transcription	K562	blood
22	chr2:169686200-169687200	Weak transcription	Fetal Intestine Small	intestine
23	chr2:169686400-169687600	Weak transcription	Left Ventricle	heart
24	chr2:169687200-169688000	ZNF genes & repeats	Adipose Nuclei	Adipose
25	chr2:169687200-169688000	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr2:169687400-169687800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr2:169687400-169688000	ZNF genes & repeats	Fetal Muscle Leg	muscle
28	chr2:169687600-169687800	ZNF genes & repeats	Right Ventricle	heart
29	chr2:169687600-169688000	ZNF genes & repeats	Left Ventricle	heart
30	chr2:169687600-169688400	Strong transcription	Lung	lung
31	chr2:169687800-169688200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
32	chr2:169687800-169692800	Weak transcription	Right Ventricle	heart
33	chr2:169688000-169689200	Weak transcription	Fetal Intestine Small	intestine
34	chr2:169688000-169691800	Weak transcription	Left Ventricle	heart
35	chr2:169688000-169693400	Strong transcription	Adipose Nuclei	Adipose
36	chr2:169688000-169705800	Weak transcription	Psoas Muscle	Psoas
37	chr2:169688000-169710600	Weak transcription	Fetal Muscle Leg	muscle
38	chr2:169688200-169690800	Strong transcription	Placenta	Placenta
39	chr2:169688200-169695400	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr2:169688400-169692600	Weak transcription	Lung	lung
41	chr2:169689000-169690400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr2:169689000-169691800	Weak transcription	Fetal Intestine Large	intestine
43	chr2:169689000-169721800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr2:169689200-169694200	Strong transcription	Fetal Intestine Small	intestine
45	chr2:169690200-169693600	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr2:169690200-169693800	Strong transcription	Pancreas	Pancrea
47	chr2:169690400-169698000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr2:169690800-169691000	Weak transcription	Placenta	Placenta
49	chr2:169690800-169694200	Strong transcription	Fetal Stomach	stomach
50	chr2:169691000-169691200	Strong transcription	Placenta	Placenta

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