Variant report

Variant	nsv521134
Chromosome Location	chr2:180746041-180848488
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:835)
CpG islands
(count:183)
Chromatin interactive
region (count:54)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:835 , 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	chr2:180818713-180819134	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:180801464-180801664	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:180812803-180813204	HepG2	liver:	n/a	n/a
4	ATF2	chr2:180817277-180817884	GM12878	blood:	n/a	n/a
5	ATF2	chr2:180817334-180817768	GM12878	blood:	n/a	n/a
6	ATF2	chr2:180816464-180816941	GM12878	blood:	n/a	n/a
7	BACH1	chr2:180809566-180809652	K562	blood:	n/a	n/a
8	BACH1	chr2:180782048-180782295	H1-hESC	embryonic stem cell:	n/a	chr2:180782187-180782201
9	BATF	chr2:180817433-180817692	GM12878	blood:	n/a	n/a
10	BCLAF1	chr2:180817353-180817781	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:180832069-180832088	K562	blood:	n/a	n/a
12	BHLHE40	chr2:180807640-180807651	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:180763202-180763282	K562	blood:	n/a	n/a
14	BHLHE40	chr2:180804153-180804320	K562	blood:	n/a	n/a
15	CBX3	chr2:180790511-180790791	K562	blood:	n/a	n/a
16	CBX3	chr2:180790429-180790754	K562	blood:	n/a	n/a
17	CBX3	chr2:180763589-180763971	HCT-116	colon:	n/a	n/a
18	CBX3	chr2:180790428-180790802	HCT-116	colon:	n/a	n/a
19	CBX3	chr2:180753394-180753724	K562	blood:	n/a	n/a
20	CBX3	chr2:180753446-180753754	K562	blood:	n/a	n/a
21	CBX3	chr2:180794756-180795038	K562	blood:	n/a	n/a
22	CCNT2	chr2:180808961-180809129	K562	blood:	n/a	n/a
23	CCNT2	chr2:180817118-180817207	K562	blood:	n/a	n/a
24	CEBPB	chr2:180818796-180819502	A549	lung:	n/a	n/a
25	CEBPB	chr2:180818828-180819092	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:180774510-180774878	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:180782089-180782308	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:180810570-180810596	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:180839562-180839829	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:180801410-180801715	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:180818801-180819489	K562	blood:	n/a	n/a
32	CEBPB	chr2:180818751-180819202	MCF-7	breast:	n/a	n/a
33	CEBPB	chr2:180828420-180828695	HepG2	liver:	n/a	chr2:180828530-180828541
34	CEBPB	chr2:180818828-180819147	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:180765724-180765949	A549	lung:	n/a	chr2:180765848-180765859
36	CEBPB	chr2:180782063-180782334	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:180828349-180828741	IMR90	lung:	n/a	chr2:180828530-180828541
38	CEBPB	chr2:180818685-180819205	A549	lung:	n/a	n/a
39	CEBPB	chr2:180828374-180828731	Hela-S3	cervix:	n/a	chr2:180828530-180828541
40	CEBPB	chr2:180765548-180766004	IMR90	lung:	n/a	chr2:180765848-180765859
41	CEBPB	chr2:180818811-180819140	IMR90	lung:	n/a	n/a
42	CEBPB	chr2:180835056-180835302	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:180818811-180819110	A549	lung:	n/a	n/a
44	CEBPB	chr2:180834998-180835302	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:180801479-180801728	MCF-7	breast:	n/a	n/a
46	CEBPB	chr2:180818719-180819528	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:180818751-180819198	MCF-7	breast:	n/a	n/a
48	CEBPB	chr2:180830694-180830954	K562	blood:	n/a	n/a
49	CEBPB	chr2:180835122-180835201	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr2:180818799-180819112	ECC-1	luminal epithelium:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:180846309-180846359	ECC-1	luminal epithelium:	n/a
2	chr2:180774797-180774847	GM19239	blood:	n/a
3	chr2:180846309-180846359	GM06990	blood:	n/a
4	chr2:180846309-180846359	HL-60	blood:	n/a
5	chr2:180846309-180846359	HPAEpiC	pulmonary alveolar:	n/a
6	chr2:180774797-180774847	T-47D	breast:	n/a
7	chr2:180846309-180846359	Hepatocyte	liver:	n/a
8	chr2:180748603-180748653	AG10803	skin:	n/a
9	chr2:180748603-180748653	MCF-7	breast:	n/a
10	chr2:180774797-180774847	HL-60	blood:	n/a
11	chr2:180774797-180774847	SK-N-SH_RA	brain:	n/a
12	chr2:180748603-180748653	NT2-D1	testis:	n/a
13	chr2:180748603-180748653	HRE	kidney:	n/a
14	chr2:180748603-180748653	HEEpiC	esophagus:	n/a
15	chr2:180774797-180774847	AoSMC	blood vessel:	n/a
16	chr2:180774797-180774847	HCPEpiC	choroid plexus:	n/a
17	chr2:180748603-180748653	Hepatocyte	liver:	n/a
18	chr2:180774797-180774847	AG04450	lung:	fetal
19	chr2:180774797-180774847	GM12878	blood:	n/a
20	chr2:180846309-180846359	ovcar-3	ovarian:	n/a
21	chr2:180846309-180846359	AG09319	gingival:	n/a
22	chr2:180774797-180774847	LNCaP	prostate:	n/a
23	chr2:180846309-180846359	MCF10A-Er-Src	breast:	n/a
24	chr2:180748603-180748653	NHDF-neo	bronchial:	n/a
25	chr2:180774797-180774847	H1-hESC	embryonic stem cell:	embryo
26	chr2:180774797-180774847	HRPEpiC	eye:	n/a
27	chr2:180748603-180748653	HCM	heart:	n/a
28	chr2:180846309-180846359	SKMC	muscle:	n/a
29	chr2:180846309-180846359	AG10803	skin:	n/a
30	chr2:180748603-180748653	BJ	skin:	n/a
31	chr2:180846309-180846359	Caco-2	colon:	n/a
32	chr2:180846309-180846359	HNPCEpiC	eye:	n/a
33	chr2:180748603-180748653	GM06990	blood:	n/a
34	chr2:180774797-180774847	CMK	blood:	n/a
35	chr2:180846309-180846359	LNCaP	prostate:	n/a
36	chr2:180774797-180774847	NHBE	bronchial:	n/a
37	chr2:180846309-180846359	PFSK-1	brain:	n/a
38	chr2:180748603-180748653	ECC-1	luminal epithelium:	n/a
39	chr2:180774797-180774847	MCF-7	breast:	n/a
40	chr2:180748603-180748653	NB4	blood:	n/a
41	chr2:180846309-180846359	AG09309	skin:	n/a
42	chr2:180748603-180748653	AG09319	gingival:	n/a
43	chr2:180774797-180774847	ProgFib	skin:	n/a
44	chr2:180774797-180774847	AG10803	skin:	n/a
45	chr2:180774797-180774847	IMR90	lung:	fetal
46	chr2:180774797-180774847	HCT-116	colon:	n/a
47	chr2:180774797-180774847	PFSK-1	brain:	n/a
48	chr2:180846309-180846359	A549	lung:	n/a
49	chr2:180846309-180846359	BJ	skin:	n/a
50	chr2:180774797-180774847	RPTEC	kidney:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:180819818..180820648-chr8:100810133..100810654,2	MCF-7	breast:
2	chr2:180816526..180819360-chr2:180870169..180871918,2	MCF-7	breast:
3	chr2:180823603..180825257-chr2:180826026..180827769,2	K562	blood:
4	chr2:180707129..180707861-chr2:180763387..180764295,2	K562	blood:
5	chr2:180816709..180819213-chr2:180821970..180823909,3	K562	blood:
6	chr2:180810995..180812628-chr2:180815849..180818711,2	K562	blood:
7	chr2:180804951..180807735-chr2:180812353..180814788,2	K562	blood:
8	chr2:180821505..180823756-chr2:180829050..180830874,2	K562	blood:
9	chr2:180808241..180810462-chr2:180810582..180812457,2	MCF-7	breast:
10	chr2:180744922..180746491-chr2:180749766..180752592,2	MCF-7	breast:
11	chr2:180810995..180812628-chr2:180815849..180818711,2	K562	blood:
12	chr2:180817808..180820267-chr2:180822152..180823709,2	MCF-7	breast:
13	chr2:180844029..180846342-chr2:180854790..180856297,2	K562	blood:
14	chr2:180743150..180746024-chr2:180754636..180757540,3	K562	blood:
15	chr2:180828855..180831224-chr2:180831279..180833933,2	MCF-7	breast:
16	chr2:180818336..180820804-chr2:180824627..180826999,2	K562	blood:
17	chr2:180818336..180820804-chr2:180824627..180826999,2	K562	blood:
18	chr2:180845616..180848330-chr2:180858035..180859969,2	K562	blood:
19	chr2:180812825..180815255-chr2:180816104..180818371,2	K562	blood:
20	chr2:180810446..180815338-chr2:180815849..180820323,6	K562	blood:
21	chr2:180771436..180773113-chr2:180774837..180777642,2	K562	blood:
22	chr2:180804951..180807735-chr2:180812353..180814788,2	K562	blood:
23	chr2:180831367..180834221-chr2:180847779..180850376,2	K562	blood:
24	chr2:180796072..180797988-chr2:180799207..180801113,2	K562	blood:
25	chr2:180800902..180803071-chr2:180803313..180806078,2	K562	blood:
26	chr2:179278797..179281186-chr2:180773348..180774954,2	K562	blood:
27	chr2:180846497..180849281-chr2:180854142..180856276,3	K562	blood:
28	chr2:180706972..180707878-chr2:180763320..180764150,2	MCF-7	breast:
29	chr2:180771436..180773113-chr2:180774837..180777642,2	K562	blood:
30	chr2:180812825..180815255-chr2:180816104..180818371,2	K562	blood:
31	chr2:180800902..180803071-chr2:180803313..180806078,2	K562	blood:
32	chr2:180843273..180847027-chr2:180868654..180873088,4	K562	blood:
33	chr2:180821505..180823756-chr2:180829050..180830874,2	K562	blood:
34	chr2:180083839..180084369-chr2:180763413..180764243,2	K562	blood:
35	chr2:180817808..180820267-chr2:180822152..180823709,2	MCF-7	breast:
36	chr2:180814982..180817147-chr2:180870910..180873047,2	K562	blood:
37	chr2:180835844..180840154-chr2:180843121..180845736,4	K562	blood:
38	chr2:179626506..179627084-chr2:180801448..180802026,2	MCF-7	breast:
39	chr2:180823603..180825257-chr2:180826026..180827769,2	K562	blood:
40	chr2:180706968..180707872-chr2:180831565..180832499,2	MCF-7	breast:
41	chr2:180810446..180815338-chr2:180815849..180820323,6	K562	blood:
42	chr2:180808241..180810462-chr2:180810582..180812457,2	MCF-7	breast:
43	chr2:180844976..180848108-chr2:180849358..180852398,4	MCF-7	breast:
44	chr2:180836754..180838955-chr2:180849215..180851382,2	K562	blood:
45	chr2:180828855..180831224-chr2:180831279..180833933,2	MCF-7	breast:
46	chr2:180813061..180815715-chr2:180844153..180846145,2	K562	blood:
47	chr2:180816709..180819213-chr2:180821970..180823909,3	K562	blood:
48	chr2:180828665..180830720-chr2:180855146..180856897,2	MCF-7	breast:
49	chr2:180744922..180746491-chr2:180749766..180752592,2	MCF-7	breast:
50	chr2:180707046..180707794-chr2:180801109..180802085,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E3-9	chr2:180808757-180808919	NONHSAT075835
2	lnc-UBE2E3-8	chr2:180800420-180800998	NONHSAT075838
3	lnc-UBE2E3-3	chr2:180782080-180782371	XLOC_001772
4	lnc-UBE2E3-3	chr2:180764787-180764889	XLOC_001772

No data

Variant related genes	Relation type
ENSG00000202216	TF binding region
ENSG00000202216	CpG island
ENSG00000163510	chromatin interactions
ENSG00000202216	chromatin interactions

Extended variants
information (count: 2950 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:2950 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11888692	chr2:180746041-180746042	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192832773	chr2:180746075-180746076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561685171	chr2:180746120-180746121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376772267	chr2:180746136-180746137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541157689	chr2:180746141-180746142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77688010	chr2:180746142-180746143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184407921	chr2:180746173-180746174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115670572	chr2:180746207-180746208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563859268	chr2:180746224-180746225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529575584	chr2:180746227-180746228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186670470	chr2:180746317-180746318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191329121	chr2:180746384-180746385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185039783	chr2:180746385-180746386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147109676	chr2:180746388-180746389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551498329	chr2:180746412-180746413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189462811	chr2:180746473-180746474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537502620	chr2:180746490-180746491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377539910	chr2:180746567-180746568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556104867	chr2:180746597-180746598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576155311	chr2:180746611-180746612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10202055	chr2:180746620-180746621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs368966006	chr2:180746635-180746636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181739349	chr2:180746662-180746663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555679964	chr2:180746696-180746697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs13016888	chr2:180746752-180746753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185131777	chr2:180746769-180746770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189654950	chr2:180746804-180746805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141432662	chr2:180746813-180746814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577667304	chr2:180746819-180746820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77704643	chr2:180746825-180746826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563763746	chr2:180746834-180746835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529425144	chr2:180746853-180746854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558844858	chr2:180746856-180746857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559608786	chr2:180746905-180746906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570966672	chr2:180746920-180746921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6744465	chr2:180746948-180746949	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs571586376	chr2:180746956-180746957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537166412	chr2:180746957-180746958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551040285	chr2:180747015-180747016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181179380	chr2:180747047-180747048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139647762	chr2:180747119-180747120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569781507	chr2:180747170-180747171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs56874518	chr2:180747179-180747180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10202606	chr2:180747180-180747181	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs75275804	chr2:180747182-180747183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572381087	chr2:180747196-180747197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185381233	chr2:180747346-180747347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557490937	chr2:180747377-180747378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577549618	chr2:180747380-180747381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543180100	chr2:180747381-180747382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

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
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
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180743200-180747000	Weak transcription	Brain Anterior Caudate	brain
2	chr2:180743200-180749000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr2:180745800-180746600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:180746600-180748200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:180746800-180747200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:180747000-180747400	Enhancers	Brain Anterior Caudate	brain
7	chr2:180747200-180748600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:180747400-180747600	Weak transcription	Brain Anterior Caudate	brain
9	chr2:180747400-180749200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr2:180747600-180748000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr2:180747600-180748000	Enhancers	Brain Anterior Caudate	brain
12	chr2:180748000-180748400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:180748200-180749200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:180748400-180748800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:180748400-180749200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:180748600-180749200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:180748800-180749200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr2:180748800-180749200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:180748800-180749200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:180748800-180749200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr2:180749000-180749400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:180749000-180749600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr2:180755600-180756400	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr2:180755800-180756400	Enhancers	Fetal Brain Male	brain
25	chr2:180764400-180767600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:180768400-180768800	Weak transcription	Pancreas	Pancrea
27	chr2:180774000-180774600	Enhancers	Liver	Liver
28	chr2:180774600-180775000	Enhancers	Brain Anterior Caudate	brain
29	chr2:180774600-180775800	Flanking Active TSS	Liver	Liver
30	chr2:180774600-180776200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr2:180774800-180775200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:180774800-180775400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:180774800-180775800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:180774800-180775800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr2:180774800-180776000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr2:180774800-180776000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:180774800-180776200	Enhancers	H1 Cell Line	embryonic stem cell
38	chr2:180774800-180776200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr2:180774800-180776200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr2:180774800-180776200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr2:180775200-180776000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr2:180775800-180776800	Enhancers	Liver	Liver
43	chr2:180776000-180776600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr2:180776800-180778400	Weak transcription	Liver	Liver
45	chr2:180778400-180778800	Enhancers	Liver	Liver
46	chr2:180778400-180779000	Enhancers	HepG2	liver
47	chr2:180780000-180780600	Enhancers	Fetal Heart	heart
48	chr2:180781600-180782800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr2:180782400-180782800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:180782800-180789600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links