Variant report

Variant	nsv1012655
Chromosome Location	chr2:128306660-128352032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:662)
CpG islands
(count:732)
Chromatin interactive
region (count:40)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:128349048-128349416	HepG2	liver:	n/a	n/a
2	ATF2	chr2:128320914-128321660	GM12878	blood:	n/a	n/a
3	ATF2	chr2:128348914-128349416	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:128321060-128321609	GM12878	blood:	n/a	n/a
5	BACH1	chr2:128349033-128349329	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:128343035-128343230	K562	blood:	n/a	n/a
7	BATF	chr2:128321136-128321858	GM12878	blood:	n/a	n/a
8	BATF	chr2:128321260-128321654	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:128321108-128321562	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:128321116-128321593	GM12878	blood:	n/a	n/a
11	BCLAF1	chr2:128321005-128321709	GM12878	blood:	n/a	n/a
12	BCLAF1	chr2:128349073-128349341	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:128349045-128349370	K562	blood:	n/a	n/a
14	BHLHE40	chr2:128321075-128321680	GM12878	blood:	n/a	n/a
15	BRCA1	chr2:128318445-128318564	HepG2	liver:	n/a	n/a
16	CBX3	chr2:128348982-128349342	K562	blood:	n/a	n/a
17	CEBPB	chr2:128330615-128330620	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:128321130-128321745	GM12878	blood:	n/a	n/a
19	CEBPB	chr2:128349084-128349423	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:128349000-128349373	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr2:128317875-128318064	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:128349086-128349381	K562	blood:	n/a	n/a
23	CEBPB	chr2:128349142-128349337	HepG2	liver:	n/a	n/a
24	CEBPD	chr2:128349131-128349314	HepG2	liver:	n/a	n/a
25	CHD2	chr2:128348982-128349275	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr2:128321841-128321914	GM12878	blood:	n/a	n/a
27	CHD2	chr2:128349131-128349289	HepG2	liver:	n/a	n/a
28	CHD2	chr2:128349251-128349257	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr2:128349065-128349344	K562	blood:	n/a	n/a
30	CHD2	chr2:128321075-128321640	GM12878	blood:	n/a	n/a
31	CREB1	chr2:128348975-128349378	A549	lung:	n/a	n/a
32	CREB1	chr2:128321010-128321683	GM12878	blood:	n/a	n/a
33	CTCF	chr2:128348720-128348870	NHLF	lung:	n/a	n/a
34	CTCF	chr2:128349064-128349375	Fibrobl	skin:	n/a	chr2:128349252-128349265 chr2:128349212-128349228 chr2:128349211-128349229 chr2:128349234-128349242
35	CTCF	chr2:128332800-128332950	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr2:128324220-128324370	GM12866	blood:	n/a	n/a
37	CTCF	chr2:128332900-128333050	GM12866	blood:	n/a	n/a
38	CTCF	chr2:128321040-128321190	GM12872	blood:	n/a	n/a
39	CTCF	chr2:128332640-128332790	GM12872	blood:	n/a	n/a
40	CTCF	chr2:128324431-128324459	GM19238	blood:	n/a	n/a
41	CTCF	chr2:128348820-128348970	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr2:128332800-128332950	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr2:128348901-128349557	K562	blood:	n/a	chr2:128349252-128349265 chr2:128349212-128349228 chr2:128349211-128349229 chr2:128349234-128349242
44	CTCF	chr2:128349140-128349290	GM12875	blood:	n/a	chr2:128349252-128349265 chr2:128349212-128349228 chr2:128349211-128349229 chr2:128349234-128349242
45	CTCF	chr2:128348780-128349653	HCT-116	colon:	n/a	chr2:128349252-128349265 chr2:128349212-128349228 chr2:128349211-128349229 chr2:128349234-128349242
46	CTCF	chr2:128349093-128349335	LNCaP	prostate:	n/a	chr2:128349252-128349265 chr2:128349212-128349228 chr2:128349211-128349229 chr2:128349234-128349242
47	CTCF	chr2:128348935-128349458	A549	lung:	n/a	chr2:128349252-128349265 chr2:128349212-128349228 chr2:128349211-128349229 chr2:128349234-128349242
48	CTCF	chr2:128349140-128349290	HVMF	connective:	n/a	chr2:128349252-128349265 chr2:128349212-128349228 chr2:128349211-128349229 chr2:128349234-128349242
49	CTCF	chr2:128332700-128332850	GM12871	blood:	n/a	n/a
50	CTCF	chr2:128349140-128349290	GM12867	blood:	n/a	chr2:128349252-128349265 chr2:128349212-128349228 chr2:128349211-128349229 chr2:128349234-128349242

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:128331593-128331643	IMR90	lung:	fetal
2	chr2:128350306-128350356	HL-60	blood:	n/a
3	chr2:128334565-128334615	NH-A	brain:	n/a
4	chr2:128331478-128331528	K562	blood:	n/a
5	chr2:128350572-128350622	AG09319	gingival:	n/a
6	chr2:128348899-128348949	ECC-1	luminal epithelium:	n/a
7	chr2:128350572-128350622	GM19239	blood:	n/a
8	chr2:128350748-128350798	NHDF-neo	bronchial:	n/a
9	chr2:128331478-128331528	LNCaP	prostate:	n/a
10	chr2:128317170-128317220	HAEpiC	amniotic membrane:	n/a
11	chr2:128350306-128350356	PANC-1	pancreas:	n/a
12	chr2:128331518-128331568	SK-N-SH_RA	brain:	n/a
13	chr2:128348899-128348949	GM12878	blood:	n/a
14	chr2:128350572-128350622	BE2_C	brain:	n/a
15	chr2:128350306-128350356	NHDF-neo	bronchial:	n/a
16	chr2:128317170-128317220	SKMC	muscle:	n/a
17	chr2:128317170-128317220	SK-N-MC	brain:	n/a
18	chr2:128347901-128347951	HCM	heart:	n/a
19	chr2:128334565-128334615	K562	blood:	n/a
20	chr2:128351542-128351592	HMEC	breast:	n/a
21	chr2:128347901-128347951	BE2_C	brain:	n/a
22	chr2:128331478-128331528	HPAEpiC	pulmonary alveolar:	n/a
23	chr2:128350306-128350356	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:128351542-128351592	HRPEpiC	eye:	n/a
25	chr2:128331593-128331643	AG09319	gingival:	n/a
26	chr2:128347901-128347951	NH-A	brain:	n/a
27	chr2:128350306-128350356	ECC-1	luminal epithelium:	n/a
28	chr2:128350572-128350622	NH-A	brain:	n/a
29	chr2:128350748-128350798	AG04450	lung:	fetal
30	chr2:128350572-128350622	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:128317170-128317220	HCT-116	colon:	n/a
32	chr2:128350442-128350492	SK-N-SH	brain:	n/a
33	chr2:128351542-128351592	HCM	heart:	n/a
34	chr2:128317170-128317220	HL-60	blood:	n/a
35	chr2:128350306-128350356	RPTEC	kidney:	n/a
36	chr2:128350442-128350492	GM19239	blood:	n/a
37	chr2:128350442-128350492	Jurkat	blood:	n/a
38	chr2:128347901-128347951	GM12891	blood:	n/a
39	chr2:128331593-128331643	GM06990	blood:	n/a
40	chr2:128317170-128317220	GM06990	blood:	n/a
41	chr2:128334565-128334615	Caco-2	colon:	n/a
42	chr2:128350572-128350622	K562	blood:	n/a
43	chr2:128331593-128331643	AG09309	skin:	n/a
44	chr2:128350572-128350622	HCF	heart:	n/a
45	chr2:128334565-128334615	RPTEC	kidney:	n/a
46	chr2:128350306-128350356	HRPEpiC	eye:	n/a
47	chr2:128331518-128331568	Hepatocyte	liver:	n/a
48	chr2:128334565-128334615	SK-N-SH_RA	brain:	n/a
49	chr2:128350306-128350356	HRCEpiC	kidney:	n/a
50	chr2:128350442-128350492	U87	brain:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:128334136..128336410-chr2:128339156..128341197,2	MCF-7	breast:
2	chr2:128336062..128337823-chr2:128338905..128341010,2	K562	blood:
3	chr2:128282885..128284606-chr2:128326771..128328709,2	MCF-7	breast:
4	chr2:128305790..128308359-chr2:128310339..128312423,2	K562	blood:
5	chr2:128334136..128336410-chr2:128339156..128341197,2	MCF-7	breast:
6	chr2:128341026..128343432-chr2:128406208..128408267,2	MCF-7	breast:
7	chr2:128340070..128342294-chr2:128344591..128347137,2	K562	blood:
8	chr2:128318000..128319961-chr2:128323554..128326504,2	K562	blood:
9	chr2:128317558..128319788-chr2:128331123..128332955,2	K562	blood:
10	chr2:128345319..128347126-chr2:128457834..128460214,2	K562	blood:
11	chr2:128282354..128284534-chr2:128320626..128323207,2	K562	blood:
12	chr2:128348778..128349285-chr2:128408202..128409066,2	K562	blood:
13	chr2:128331003..128333151-chr2:128458279..128460018,2	MCF-7	breast:
14	chr2:128336968..128338613-chr2:128421109..128423481,2	K562	blood:
15	chr2:128349107..128352400-chr2:128458285..128460511,3	MCF-7	breast:
16	chr2:128281670..128284609-chr2:128307650..128309640,2	K562	blood:
17	chr2:128349507..128351016-chr2:128354758..128356667,2	K562	blood:
18	chr2:128349069..128349649-chr2:128452945..128453583,3	MCF-7	breast:
19	chr2:128330113..128332946-chr2:128335527..128337654,2	K562	blood:
20	chr2:128289324..128291170-chr2:128329795..128331725,2	MCF-7	breast:
21	chr2:128330113..128332946-chr2:128335527..128337654,2	K562	blood:
22	chr2:128336062..128337823-chr2:128338905..128341010,2	K562	blood:
23	chr2:128348782..128349711-chr2:128407012..128408114,6	MCF-7	breast:
24	chr2:128283723..128286388-chr2:128321696..128326699,5	MCF-7	breast:
25	chr2:128318000..128319961-chr2:128323554..128326504,2	K562	blood:
26	chr2:128349017..128351644-chr2:128387621..128389792,2	MCF-7	breast:
27	chr2:128305790..128308359-chr2:128310339..128312423,2	K562	blood:
28	chr2:128350066..128351938-chr2:128352163..128353978,2	MCF-7	breast:
29	chr2:128348828..128349586-chr2:128398143..128398870,2	MCF-7	breast:
30	chr2:128286477..128289407-chr2:128321219..128322909,3	MCF-7	breast:
31	chr2:128348935..128349717-chr2:128397753..128398634,2	MCF-7	breast:
32	chr2:128344046..128345819-chr2:128458490..128460520,2	MCF-7	breast:
33	chr2:128283130..128286145-chr2:128334041..128336604,3	K562	blood:
34	chr2:128340070..128342294-chr2:128344591..128347137,2	K562	blood:
35	chr2:128317558..128319788-chr2:128331123..128332955,2	K562	blood:
36	chr2:128348763..128349664-chr2:128408092..128409288,3	MCF-7	breast:
37	chr2:128349348..128351904-chr2:128462965..128465382,2	MCF-7	breast:
38	chr2:128348736..128349703-chr2:128407022..128407964,6	K562	blood:
39	chr2:128338620..128340523-chr2:128457766..128459740,2	MCF-7	breast:
40	chr2:128348754..128349757-chr2:128407019..128407967,16	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IWS1-1	chr2:128322263-128322364	ENSG00000250457
2	lnc-IWS1-1	chr2:128317620-128319553	ENSG00000250457
3	lnc-IWS1-1	chr2:128318774-128319641	ucscGeneNc_uc010fmc_1
4	lnc-IWS1-1	chr2:128317597-128318108	ucscGeneNc_uc010fmc_1
5	lnc-LIMS2-3	chr2:128345637-128345930	expReg_chr2_9243_-

No data

Variant related genes	Relation type
MYO7B	TF binding region
MYO7B	CpG island
ENSG00000163166	chromatin interactions
ENSG00000144230	chromatin interactions
ENSG00000173349	chromatin interactions
ENSG00000072163	chromatin interactions
RTN4	miRNA target sites
DDX10	miRNA target sites

Extended variants
information (count: 1951 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1951 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530271875	chr2:128306685-128306686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192814487	chr2:128306691-128306692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144569162	chr2:128306703-128306704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374377593	chr2:128306706-128306707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370724652	chr2:128306710-128306711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546378842	chr2:128306722-128306723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199598753	chr2:128306723-128306724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs386650230	chr2:128306734-128306735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143181627	chr2:128306735-128306736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560033807	chr2:128306738-128306739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71841221	chr2:128306739-128306740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112772817	chr2:128306742-128306743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566542590	chr2:128306749-128306750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs202056688	chr2:128306754-128306755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200632902	chr2:128306758-128306759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73953640	chr2:128306761-128306762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532159607	chr2:128306783-128306784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184678631	chr2:128306788-128306789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569201017	chr2:128306812-128306813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537744899	chr2:128306828-128306829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554809838	chr2:128306865-128306866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189425901	chr2:128306909-128306910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181946769	chr2:128306945-128306946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553066195	chr2:128306983-128306984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76580265	chr2:128306996-128306997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572988612	chr2:128307002-128307003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545032377	chr2:128307077-128307078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184210439	chr2:128307081-128307082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537848801	chr2:128307082-128307083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575936196	chr2:128307097-128307098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372688385	chr2:128307125-128307126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544586278	chr2:128307134-128307135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188964346	chr2:128307194-128307195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150114114	chr2:128307211-128307212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531278560	chr2:128307228-128307229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540793605	chr2:128307267-128307268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538301908	chr2:128307293-128307294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62156600	chr2:128307356-128307357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560323317	chr2:128307365-128307366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532221930	chr2:128307367-128307368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181099348	chr2:128307380-128307381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374496695	chr2:128307381-128307382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145376605	chr2:128307544-128307545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531290957	chr2:128307574-128307575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116245990	chr2:128307587-128307588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568311179	chr2:128307589-128307590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17015401	chr2:128307591-128307592	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs186749397	chr2:128307686-128307687	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs539082718	chr2:128307697-128307698	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190739473	chr2:128307701-128307702	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:128284600-128321200	Weak transcription	Spleen	Spleen
2	chr2:128300200-128320600	Weak transcription	Colonic Mucosa	Colon
3	chr2:128300600-128307200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr2:128301400-128317000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr2:128304800-128307200	Weak transcription	Fetal Intestine Small	intestine
6	chr2:128305200-128318200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr2:128305400-128307000	Weak transcription	Fetal Intestine Large	intestine
8	chr2:128307000-128310800	Strong transcription	Fetal Intestine Large	intestine
9	chr2:128307200-128309600	Strong transcription	Duodenum Mucosa	Duodenum
10	chr2:128307200-128310800	Strong transcription	Fetal Intestine Small	intestine
11	chr2:128309200-128309600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr2:128309600-128313600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr2:128310000-128315000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr2:128310800-128316000	Weak transcription	Fetal Intestine Large	intestine
15	chr2:128310800-128316400	Weak transcription	Fetal Intestine Small	intestine
16	chr2:128313600-128314000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
17	chr2:128314000-128316600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr2:128315000-128315400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
19	chr2:128315400-128321000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr2:128316000-128316600	Enhancers	NHEK	skin
21	chr2:128316000-128319600	Strong transcription	Fetal Intestine Large	intestine
22	chr2:128316400-128319200	Strong transcription	Fetal Intestine Small	intestine
23	chr2:128316600-128316800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:128316600-128317000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:128316600-128318000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:128316600-128318400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr2:128316600-128319600	Strong transcription	Duodenum Mucosa	Duodenum
28	chr2:128316800-128317200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr2:128316800-128317400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:128316800-128317400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:128316800-128317600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:128316800-128318400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr2:128317000-128317200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr2:128317000-128317600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:128317000-128318800	Strong transcription	Rectal Mucosa Donor 29	rectum
36	chr2:128317200-128317600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:128317200-128318000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:128317200-128318200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr2:128317200-128319800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:128317400-128317800	Enhancers	Muscle Satellite Cultured Cells	--
41	chr2:128317400-128317800	Enhancers	Osteobl	bone
42	chr2:128317400-128320000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:128317600-128317800	Bivalent Enhancer	HepG2	liver
44	chr2:128317600-128318000	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr2:128317600-128318000	Enhancers	HSMM	muscle
46	chr2:128317600-128318400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:128317800-128318800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr2:128317800-128318800	Flanking Bivalent TSS/Enh	HepG2	liver
49	chr2:128317800-128318800	Enhancers	HSMMtube	muscle
50	chr2:128317800-128318800	Flanking Active TSS	Osteobl	bone

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