Variant report

Variant	nsv874270
Chromosome Location	chr2:73837751-73916672
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1202)
CpG islands
(count:1103)
Chromatin interactive
region (count:27)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73857942-73858125	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
6	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
7	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
8	BACH1	chr2:73857107-73857303	K562	blood:	n/a	n/a
9	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
11	BATF	chr2:73851315-73851489	GM12878	blood:	n/a	chr2:73851419-73851430
12	BATF	chr2:73851278-73851536	GM12878	blood:	n/a	chr2:73851419-73851430
13	BATF	chr2:73855647-73855936	GM12878	blood:	n/a	n/a
14	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
15	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
16	BCL11A	chr2:73855638-73856013	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:73915732-73916019	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
19	BHLHE40	chr2:73837637-73837780	K562	blood:	n/a	n/a
20	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
21	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
22	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
24	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
25	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
26	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
27	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
28	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
29	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
30	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
31	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr2:73838631-73838706	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
36	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
39	CEBPB	chr2:73841359-73841438	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
42	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
43	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
44	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
45	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
46	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
47	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
48	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
49	CTCF	chr2:73891902-73891943	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr2:73912078-73912338	MCF-7	breast:	n/a	n/a

(count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73871942-73871992	MCF-7	breast:	n/a
2	chr2:73870653-73870703	LNCaP	prostate:	n/a
3	chr2:73871855-73871905	ECC-1	luminal epithelium:	n/a
4	chr2:73871915-73871965	GM06990	blood:	n/a
5	chr2:73868736-73868786	HL-60	blood:	n/a
6	chr2:73871942-73871992	MCF-7	breast:	n/a
7	chr2:73870653-73870703	LNCaP	prostate:	n/a
8	chr2:73871855-73871905	ECC-1	luminal epithelium:	n/a
9	chr2:73871915-73871965	GM06990	blood:	n/a
10	chr2:73868736-73868786	HL-60	blood:	n/a
11	chr2:73870653-73870703	HAEpiC	amniotic membrane:	n/a
12	chr2:73869666-73869716	GM06990	blood:	n/a
13	chr2:73868919-73868969	NH-A	brain:	n/a
14	chr2:73869966-73870016	A549	lung:	n/a
15	chr2:73870294-73870344	HMEC	breast:	n/a
16	chr2:73871855-73871905	NH-A	brain:	n/a
17	chr2:73871782-73871832	H1-hESC	embryonic stem cell:	embryo
18	chr2:73868917-73868967	GM06990	blood:	n/a
19	chr2:73869666-73869716	HUVEC	blood vessel:	n/a
20	chr2:73868917-73868967	HAEpiC	amniotic membrane:	n/a
21	chr2:73870653-73870703	AoSMC	blood vessel:	n/a
22	chr2:73871309-73871359	Hela-S3	cervix:	n/a
23	chr2:73870294-73870344	AG10803	skin:	n/a
24	chr2:73871855-73871905	HCT-116	colon:	n/a
25	chr2:73868919-73868969	AG10803	skin:	n/a
26	chr2:73871849-73871899	HCT-116	colon:	n/a
27	chr2:73907327-73907377	HRPEpiC	eye:	n/a
28	chr2:73871855-73871905	SK-N-SH	brain:	n/a
29	chr2:73871855-73871905	PANC-1	pancreas:	n/a
30	chr2:73870653-73870703	IMR90	lung:	fetal
31	chr2:73867196-73867246	AG09309	skin:	n/a
32	chr2:73907327-73907377	CMK	blood:	n/a
33	chr2:73871230-73871280	HCPEpiC	choroid plexus:	n/a
34	chr2:73868917-73868967	HRE	kidney:	n/a
35	chr2:73867196-73867246	A549	lung:	n/a
36	chr2:73871915-73871965	PANC-1	pancreas:	n/a
37	chr2:73871782-73871832	AG04450	lung:	fetal
38	chr2:73868919-73868969	AoSMC	blood vessel:	n/a
39	chr2:73867196-73867246	NB4	blood:	n/a
40	chr2:73871230-73871280	HepG2	liver:	n/a
41	chr2:73871855-73871905	AG09309	skin:	n/a
42	chr2:73869516-73869566	BE2_C	brain:	n/a
43	chr2:73871309-73871359	AoSMC	blood vessel:	n/a
44	chr2:73870105-73870155	MCF10A-Er-Src	breast:	n/a
45	chr2:73869666-73869716	BE2_C	brain:	n/a
46	chr2:73871915-73871965	HCT-116	colon:	n/a
47	chr2:73871230-73871280	PrEC	prostate:	n/a
48	chr2:73871309-73871359	HEEpiC	esophagus:	n/a
49	chr2:73869666-73869716	HEK293	kidney:	embryo
50	chr2:73868917-73868967	RPTEC	kidney:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
2	chr2:73839411..73842027-chr2:73845184..73847412,3	MCF-7	breast:
3	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
4	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
5	chr2:73837883..73840443-chr2:74211046..74212867,2	MCF-7	breast:
6	chr2:73842404..73844324-chr2:73845193..73847014,2	MCF-7	breast:
7	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
8	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
9	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
10	chr2:73842508..73845608-chr2:73846002..73848469,3	K562	blood:
11	chr2:73839411..73842027-chr2:73845184..73847412,3	MCF-7	breast:
12	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
13	chr2:73842508..73845608-chr2:73846002..73848469,3	K562	blood:
14	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
15	chr2:73842404..73844324-chr2:73845193..73847014,2	MCF-7	breast:
16	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
17	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
18	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
19	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
20	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
21	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
22	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
23	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
24	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
25	chr2:73834970..73837319-chr2:73844095..73845745,2	K562	blood:
26	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
27	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
2	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
3	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
4	lnc-ALMS1-3	chr2:73912088-73912694	NR_003683
5	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
6	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
7	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
8	lnc-ALMS1-2	chr2:73868076-73868755	NONHSAT071625

No data

Variant related genes	Relation type
ALMS1P	TF binding region
NAT8	TF binding region
ALMS1P	CpG island
NAT8	CpG island
ENSG00000144048	chromatin interactions
ENSG00000235499	chromatin interactions
ENSG00000204872	chromatin interactions

Extended variants
information (count: 3066 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3066 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6546856	chr2:73837751-73837752	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116937728	chr2:73837765-73837766	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563304535	chr2:73837863-73837864	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146775626	chr2:73837877-73837878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549411521	chr2:73837902-73837903	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554127011	chr2:73837939-73837940	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs6546857	chr2:73837955-73837956	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
8	rs575658518	chr2:73838043-73838044	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs571698733	chr2:73838120-73838121	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539731708	chr2:73838136-73838137	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192018186	chr2:73838206-73838207	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573069912	chr2:73838243-73838244	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140622033	chr2:73838258-73838259	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs555397625	chr2:73838261-73838262	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374101510	chr2:73838270-73838271	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs117221166	chr2:73838277-73838278	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544166792	chr2:73838390-73838391	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183289483	chr2:73838393-73838394	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs187530188	chr2:73838420-73838421	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545285685	chr2:73838490-73838491	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560416965	chr2:73838518-73838519	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527847913	chr2:73838565-73838566	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs72913464	chr2:73838572-73838573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs6546858	chr2:73838613-73838614	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs531692106	chr2:73838625-73838626	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370967337	chr2:73838696-73838697	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs114981706	chr2:73838713-73838714	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571661579	chr2:73838752-73838753	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs137962971	chr2:73838757-73838758	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs386647344	chr2:73838758-73838759	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374149956	chr2:73838759-73838760	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs10547252	chr2:73838761-73838762	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551653100	chr2:73838780-73838781	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs550915009	chr2:73838795-73838796	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs11388758	chr2:73838802-73838803	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs386390468	chr2:73838803-73838804	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs11406153	chr2:73838805-73838806	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79055116	chr2:73838844-73838845	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs114440232	chr2:73838941-73838942	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555292280	chr2:73838948-73838949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573807109	chr2:73838990-73838991	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537528514	chr2:73839019-73839020	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs555879206	chr2:73839067-73839068	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs151098800	chr2:73839069-73839070	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35284464	chr2:73839074-73839075	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs190489707	chr2:73839080-73839081	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141038420	chr2:73839090-73839091	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs536639388	chr2:73839190-73839191	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560381854	chr2:73839196-73839197	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572673886	chr2:73839198-73839199	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
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
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73765800-73837800	Weak transcription	Fetal Brain Male	brain
2	chr2:73785400-73838200	Weak transcription	Psoas Muscle	Psoas
3	chr2:73801000-73844000	Weak transcription	Fetal Kidney	kidney
4	chr2:73822000-73838800	Weak transcription	Fetal Heart	heart
5	chr2:73822600-73840800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:73823000-73844600	Weak transcription	Primary B cells from cord blood	blood
7	chr2:73826000-73841200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr2:73826200-73841400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:73826600-73839200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr2:73826800-73838800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr2:73827000-73840600	Weak transcription	NHLF	lung
12	chr2:73827600-73838200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:73827600-73839200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:73827800-73840400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr2:73828800-73837800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr2:73829000-73839000	Weak transcription	NHDF-Ad	bronchial
17	chr2:73829000-73839400	Weak transcription	Placenta	Placenta
18	chr2:73829200-73838600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:73829200-73840000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr2:73829400-73845400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr2:73829600-73840200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr2:73829800-73838000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr2:73829800-73839600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:73829800-73840000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr2:73829800-73840000	Weak transcription	Gastric	stomach
26	chr2:73829800-73840400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:73830000-73840800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr2:73830200-73838000	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr2:73830400-73839200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr2:73830400-73843600	Weak transcription	Aorta	Aorta
31	chr2:73830600-73838000	Weak transcription	GM12878-XiMat	blood
32	chr2:73830600-73838000	Weak transcription	HSMMtube	muscle
33	chr2:73830600-73838800	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr2:73830600-73839000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:73830600-73839000	Weak transcription	Primary B cells from peripheral blood	blood
36	chr2:73830600-73839600	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr2:73830600-73840000	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr2:73830600-73841200	Weak transcription	Liver	Liver
39	chr2:73830600-73843000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr2:73830600-73847600	Weak transcription	Spleen	Spleen
41	chr2:73830600-73854800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr2:73830800-73837800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:73830800-73839200	Weak transcription	Osteobl	bone
44	chr2:73830800-73840800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr2:73831000-73837800	Weak transcription	Brain Substantia Nigra	brain
46	chr2:73831000-73838000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr2:73831000-73842200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:73831200-73839600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr2:73831200-73841200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr2:73832600-73838000	Weak transcription	Brain Angular Gyrus	brain

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