Variant report

Variant	nsv874781
Chromosome Location	chr2:110463288-110804164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3144)
CpG islands
(count:245)
Chromatin interactive
region (count:7)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:3144 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:110472920-110473302	HepG2	liver:	n/a	n/a
2	BACH1	chr2:110493854-110494137	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:110595079-110595276	GM12878	blood:	n/a	n/a
4	BATF	chr2:110653650-110654385	GM12878	blood:	n/a	chr2:110654054-110654064 chr2:110654053-110654064
5	BATF	chr2:110663352-110663813	GM12878	blood:	n/a	chr2:110663553-110663564 chr2:110663608-110663619
6	BATF	chr2:110594892-110595317	GM12878	blood:	n/a	n/a
7	BATF	chr2:110554721-110555155	GM12878	blood:	n/a	n/a
8	BATF	chr2:110519533-110520254	GM12878	blood:	n/a	n/a
9	BATF	chr2:110645180-110645680	GM12878	blood:	n/a	n/a
10	BATF	chr2:110555685-110555899	GM12878	blood:	n/a	n/a
11	BATF	chr2:110738365-110738645	GM12878	blood:	n/a	n/a
12	BATF	chr2:110655074-110655448	GM12878	blood:	n/a	n/a
13	BATF	chr2:110591595-110591865	GM12878	blood:	n/a	n/a
14	BATF	chr2:110645383-110645632	GM12878	blood:	n/a	n/a
15	BATF	chr2:110662784-110663052	GM12878	blood:	n/a	chr2:110662929-110662940
16	BATF	chr2:110628682-110629136	GM12878	blood:	n/a	n/a
17	BATF	chr2:110552518-110552811	GM12878	blood:	n/a	n/a
18	BATF	chr2:110733954-110734198	GM12878	blood:	n/a	n/a
19	BATF	chr2:110515529-110515864	GM12878	blood:	n/a	n/a
20	BATF	chr2:110653035-110653493	GM12878	blood:	n/a	n/a
21	BATF	chr2:110597287-110597588	GM12878	blood:	n/a	n/a
22	BATF	chr2:110519567-110520304	GM12878	blood:	n/a	n/a
23	BATF	chr2:110653717-110654248	GM12878	blood:	n/a	chr2:110654054-110654064 chr2:110654053-110654064
24	BATF	chr2:110592910-110593154	GM12878	blood:	n/a	n/a
25	BATF	chr2:110565195-110565489	GM12878	blood:	n/a	n/a
26	BATF	chr2:110596705-110596958	GM12878	blood:	n/a	n/a
27	BATF	chr2:110550261-110550597	GM12878	blood:	n/a	n/a
28	BATF	chr2:110596658-110596861	GM12878	blood:	n/a	n/a
29	BATF	chr2:110663321-110663821	GM12878	blood:	n/a	chr2:110663553-110663564 chr2:110663608-110663619
30	BATF	chr2:110554663-110555199	GM12878	blood:	n/a	n/a
31	BATF	chr2:110628689-110629008	GM12878	blood:	n/a	n/a
32	BATF	chr2:110551684-110552114	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:110622746-110622931	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:110554748-110555164	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:110605050-110605227	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:110515454-110515890	GM12878	blood:	n/a	chr2:110515591-110515600 chr2:110515592-110515601
37	BCL11A	chr2:110552372-110552860	GM12878	blood:	n/a	chr2:110552563-110552572
38	BCL11A	chr2:110653735-110654258	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:110519679-110520200	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:110653076-110653477	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:110653775-110654123	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:110615296-110615523	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:110519572-110520290	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:110552529-110552917	GM12878	blood:	n/a	chr2:110552563-110552572
45	BCL11A	chr2:110514007-110514230	GM12878	blood:	n/a	chr2:110514163-110514172
46	BCL11A	chr2:110608683-110608858	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:110653155-110653347	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:110663268-110663851	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:110602022-110602295	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:110738261-110738582	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:110706159-110706209	GM06990	blood:	n/a
2	chr2:110706159-110706209	GM06990	blood:	n/a
3	chr2:110521111-110521161	Jurkat	blood:	n/a
4	chr2:110705781-110705831	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:110705781-110705831	ProgFib	skin:	n/a
6	chr2:110518888-110518938	HAEpiC	amniotic membrane:	n/a
7	chr2:110706159-110706209	HepG2	liver:	n/a
8	chr2:110705781-110705831	HCF	heart:	n/a
9	chr2:110705781-110705831	AG10803	skin:	n/a
10	chr2:110705781-110705831	HEK293	kidney:	embryo
11	chr2:110705781-110705831	U87	brain:	n/a
12	chr2:110705781-110705831	ovcar-3	ovarian:	n/a
13	chr2:110518888-110518938	BE2_C	brain:	n/a
14	chr2:110521111-110521161	PANC-1	pancreas:	n/a
15	chr2:110706159-110706209	AoSMC	blood vessel:	n/a
16	chr2:110705781-110705831	HIPEpiC	eye:	n/a
17	chr2:110705781-110705831	SK-N-MC	brain:	n/a
18	chr2:110706159-110706209	HCF	heart:	n/a
19	chr2:110521111-110521161	CMK	blood:	n/a
20	chr2:110705781-110705831	HAEpiC	amniotic membrane:	n/a
21	chr2:110521111-110521161	NHBE	bronchial:	n/a
22	chr2:110706159-110706209	RPTEC	kidney:	n/a
23	chr2:110518888-110518938	SK-N-SH_RA	brain:	n/a
24	chr2:110706159-110706209	GM12892	blood:	n/a
25	chr2:110706159-110706209	HNPCEpiC	eye:	n/a
26	chr2:110518888-110518938	Hela-S3	cervix:	n/a
27	chr2:110518888-110518938	IMR90	lung:	fetal
28	chr2:110705781-110705831	IMR90	lung:	fetal
29	chr2:110521111-110521161	AoSMC	blood vessel:	n/a
30	chr2:110705781-110705831	HepG2	liver:	n/a
31	chr2:110705781-110705831	HEEpiC	esophagus:	n/a
32	chr2:110706159-110706209	Caco-2	colon:	n/a
33	chr2:110706159-110706209	Hepatocyte	liver:	n/a
34	chr2:110705781-110705831	SAEC	small airway:	n/a
35	chr2:110518888-110518938	HUVEC	blood vessel:	n/a
36	chr2:110518888-110518938	NHBE	bronchial:	n/a
37	chr2:110521111-110521161	AG09309	skin:	n/a
38	chr2:110705781-110705831	K562	blood:	n/a
39	chr2:110705781-110705831	RPTEC	kidney:	n/a
40	chr2:110521111-110521161	SK-N-SH_RA	brain:	n/a
41	chr2:110705781-110705831	A549	lung:	n/a
42	chr2:110518888-110518938	ovcar-3	ovarian:	n/a
43	chr2:110518888-110518938	HRPEpiC	eye:	n/a
44	chr2:110706159-110706209	LNCaP	prostate:	n/a
45	chr2:110705781-110705831	NH-A	brain:	n/a
46	chr2:110518888-110518938	NHDF-neo	bronchial:	n/a
47	chr2:110706159-110706209	Hela-S3	cervix:	n/a
48	chr2:110518888-110518938	PrEC	prostate:	n/a
49	chr2:110521111-110521161	HRPEpiC	eye:	n/a
50	chr2:110706159-110706209	HPAEpiC	pulmonary alveolar:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:110303649..110304318-chr2:110493558..110494245,2	K562	blood:
2	chr2:110273703..110274218-chr2:110493544..110494330,2	MCF-7	breast:
3	chr2:110456223..110458678-chr2:110473323..110476138,2	MCF-7	breast:
4	chr2:110303139..110304334-chr2:110493545..110494430,6	MCF-7	breast:
5	chr2:110369598..110371747-chr2:110472981..110475520,2	MCF-7	breast:
6	chr2:110369302..110370206-chr2:110472595..110473565,2	MCF-7	breast:
7	chr2:110273525..110274131-chr2:110493868..110494433,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIMS3-1	chr2:110745138-110745187	NONHSAT073165
2	lnc-LIMS3-1	chr2:110745849-110746379	ENSG00000204588
3	lnc-LIMS3.1-2	chr2:110595460-110595619	NONHSAT073153
4	lnc-RGPD5-1	chr2:110490308-110490713	NONHSAT073149
5	lnc-LIMS3.1-2	chr2:110596511-110596570	NONHSAT073153
6	lnc-LIMS3-1	chr2:110746130-110746278	NONHSAT073165
7	lnc-SEPT10-2	chr2:110595035-110595535	ucscGeneNc_uc010fjz_1
8	lnc-SEPT10-2	chr2:110598802-110598916	ucscGeneNc_uc010fjz_1
9	lnc-MALL-3	chr2:110769842-110770178	NONHSAT073169
10	lnc-LIMS3-1	chr2:110751978-110752031	NONHSAT073165
11	lnc-SEPT10-2	chr2:110615775-110615987	ucscGeneNc_uc010fjz_1
12	lnc-LIMS3-1	chr2:110746317-110746379	NONHSAT073165
13	lnc-LIMS3-1	chr2:110751978-110753717	ENSG00000204588
14	lnc-LIMS3-1	chr2:110744703-110744767	NONHSAT073165

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	RGPD6	hsa-miR-15a-5p	chr2:110614843-110614864
2	RGPD6	hsa-miR-15a-5p	chr2:110615252-110615272
3	RGPD5	hsa-miR-335-5p	chr2:110614364-110614387

Variant related genes	Relation type
ENSG00000235721	TF binding region
ENSG00000229730	TF binding region
GPAA1P1	TF binding region
RPL22P11	TF binding region
ENSG00000233307	TF binding region
LINC01123	TF binding region
ENSG00000186148	TF binding region
LIMS3	TF binding region
RGPD5	TF binding region
ZBTB45P1	TF binding region
ENSG00000235721	CpG island
ENSG00000229730	CpG island
GPAA1P1	CpG island
RPL22P11	CpG island
ENSG00000233307	CpG island
LINC01123	CpG island
ENSG00000186148	CpG island
LIMS3	CpG island
RGPD5	CpG island
ZBTB45P1	CpG island
ENSG00000186522	chromatin interactions

Extended variants
information (count: 1294 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1294 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34229733	chr2:110463288-110463289	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531811165	chr2:110463304-110463305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186999601	chr2:110463314-110463315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564156363	chr2:110463358-110463359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372872658	chr2:110463384-110463385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533085954	chr2:110463385-110463386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62151726	chr2:110463422-110463423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559905333	chr2:110463460-110463461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376644301	chr2:110463478-110463479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541568824	chr2:110463509-110463510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529146003	chr2:110463547-110463548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144704376	chr2:110463610-110463611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569178306	chr2:110463619-110463620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537634195	chr2:110463655-110463656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191537512	chr2:110463702-110463703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571380378	chr2:110463732-110463733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534043164	chr2:110463741-110463742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553710375	chr2:110463775-110463776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566290408	chr2:110463785-110463786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146661124	chr2:110463791-110463792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140216455	chr2:110463800-110463801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535329128	chr2:110463811-110463812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11682853	chr2:110463824-110463825	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs576709522	chr2:110463843-110463844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545593358	chr2:110463844-110463845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138303185	chr2:110463942-110463943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183449242	chr2:110464010-110464011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540337834	chr2:110464035-110464036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547422091	chr2:110464036-110464037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149643325	chr2:110464080-110464081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187893692	chr2:110464082-110464083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562623872	chr2:110464171-110464172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559337812	chr2:110464174-110464175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191540808	chr2:110464186-110464187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571119057	chr2:110464259-110464260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533984638	chr2:110464263-110464264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547484991	chr2:110464308-110464309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35293316	chr2:110464361-110464362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs148362490	chr2:110464389-110464390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182273577	chr2:110464433-110464434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34463187	chr2:110464452-110464453	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186472966	chr2:110464470-110464471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192540384	chr2:110464504-110464505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572678608	chr2:110464505-110464506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185526156	chr2:110464517-110464518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559980935	chr2:110464637-110464638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573713131	chr2:110464644-110464645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542231310	chr2:110464693-110464694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562520912	chr2:110464725-110464726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531462714	chr2:110464726-110464727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Autism	17483303	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
Ovarian cancer	21781307	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495309	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
Autism	22549408	CNVD
Autism	21865298	CNVD
small cell lung cancer	20016488	CNVD
Disease	19212409	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110458800-110468400	Weak transcription	Right Atrium	heart
2	chr2:110460200-110464000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:110460200-110468800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:110460200-110469200	Weak transcription	Lung	lung
5	chr2:110460400-110467000	Weak transcription	Stomach Mucosa	stomach
6	chr2:110460600-110465000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:110461000-110467000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr2:110461000-110474200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr2:110461200-110467000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr2:110461400-110464600	Weak transcription	Fetal Lung	lung
11	chr2:110462000-110464400	Weak transcription	Esophagus	oesophagus
12	chr2:110462000-110469000	Weak transcription	HepG2	liver
13	chr2:110463000-110463400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:110463000-110463800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr2:110463000-110464200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr2:110463000-110464600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr2:110463200-110464000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr2:110463200-110464200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:110464000-110464200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:110464400-110466200	Enhancers	Esophagus	oesophagus
21	chr2:110464600-110468200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr2:110465000-110465400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:110466200-110473000	Weak transcription	Esophagus	oesophagus
24	chr2:110467000-110467200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr2:110467000-110467200	Enhancers	Stomach Mucosa	stomach
26	chr2:110467000-110467400	Enhancers	Duodenum Mucosa	Duodenum
27	chr2:110467000-110467600	Enhancers	Colonic Mucosa	Colon
28	chr2:110467000-110467600	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr2:110467000-110468600	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr2:110467000-110470000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr2:110467200-110468000	Weak transcription	Stomach Mucosa	stomach
32	chr2:110467200-110468200	Weak transcription	Spleen	Spleen
33	chr2:110468000-110468400	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr2:110468000-110468400	Enhancers	Stomach Mucosa	stomach
35	chr2:110468000-110469800	Enhancers	Fetal Heart	heart
36	chr2:110468200-110468400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr2:110468200-110468600	Enhancers	Spleen	Spleen
38	chr2:110468400-110468800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:110468400-110469600	Enhancers	Right Atrium	heart
40	chr2:110468600-110469600	Enhancers	Right Ventricle	heart
41	chr2:110468600-110472800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr2:110468800-110469200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:110468800-110469200	Enhancers	Left Ventricle	heart
44	chr2:110468800-110469600	Enhancers	Placenta	Placenta
45	chr2:110468800-110469800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:110468800-110469800	Enhancers	GM12878-XiMat	blood
47	chr2:110468800-110484400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:110469000-110469200	Active TSS	HepG2	liver
49	chr2:110469000-110469400	Enhancers	Stomach Smooth Muscle	stomach
50	chr2:110469000-110469800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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