Variant report

Variant	esv3327699
Chromosome Location	chr2:110462513-110519411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	chr2:110515529-110515864	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:110514007-110514230	GM12878	blood:	n/a	chr2:110514163-110514172
5	BCL11A	chr2:110515454-110515890	GM12878	blood:	n/a	chr2:110515591-110515600 chr2:110515592-110515601
6	BCL11A	chr2:110515524-110515815	GM12878	blood:	n/a	chr2:110515591-110515600 chr2:110515592-110515601
7	BCL3	chr2:110468497-110468769	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:110484123-110484277	K562	blood:	n/a	n/a
9	BRCA1	chr2:110472985-110473242	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr2:110493847-110494110	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:110476190-110476272	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:110469467-110469797	HepG2	liver:	n/a	chr2:110469625-110469636
13	CEBPB	chr2:110515481-110516035	GM12878	blood:	n/a	chr2:110515496-110515507 chr2:110515494-110515507
14	CEBPB	chr2:110472847-110473287	HepG2	liver:	n/a	n/a
15	CHD2	chr2:110479356-110479464	HepG2	liver:	n/a	n/a
16	CTCF	chr2:110478901-110478965	NHEK	skin:	n/a	n/a
17	CTCF	chr2:110473060-110473210	HA-sp	spinal cord:	n/a	n/a
18	CTCF	chr2:110493940-110494090	HMEC	breast:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
19	CTCF	chr2:110473011-110473234	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr2:110493900-110494050	HEEpiC	esophagus:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
21	CTCF	chr2:110505100-110505250	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr2:110493800-110493950	GM12866	blood:	n/a	n/a
23	CTCF	chr2:110500769-110500809	MCF-7	breast:	n/a	n/a
24	CTCF	chr2:110493905-110494063	SK-N-SH_RA	brain:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
25	CTCF	chr2:110493820-110493970	AG09319	gingival:	n/a	n/a
26	CTCF	chr2:110493820-110493970	NHEK	skin:	n/a	n/a
27	CTCF	chr2:110473060-110473210	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr2:110473100-110473250	HCT-116	colon:	n/a	n/a
29	CTCF	chr2:110478400-110478550	HMEC	breast:	n/a	n/a
30	CTCF	chr2:110493880-110494030	GM12870	blood:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
31	CTCF	chr2:110468420-110468570	GM12873	blood:	n/a	n/a
32	CTCF	chr2:110473020-110473275	K562	blood:	n/a	n/a
33	CTCF	chr2:110473080-110473230	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr2:110493839-110494165	K562	blood:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
35	CTCF	chr2:110493820-110493970	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr2:110493920-110494070	GM12864	blood:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
37	CTCF	chr2:110473040-110473190	GM12872	blood:	n/a	n/a
38	CTCF	chr2:110493900-110494050	GM12869	blood:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
39	CTCF	chr2:110473040-110473190	GM12878	blood:	n/a	n/a
40	CTCF	chr2:110473060-110473210	HMF	breast:	n/a	n/a
41	CTCF	chr2:110493860-110494010	RPTEC	kidney:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
42	CTCF	chr2:110493801-110494053	H1-hESC	embryonic stem cell:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
43	CTCF	chr2:110493848-110494166	A549	lung:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
44	CTCF	chr2:110491196-110491232	GM13977	blood:	n/a	n/a
45	CTCF	chr2:110473040-110473190	GM12865	blood:	n/a	n/a
46	CTCF	chr2:110473080-110473230	GM12873	blood:	n/a	n/a
47	CTCF	chr2:110493860-110494010	GM12873	blood:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
48	CTCF	chr2:110493880-110494030	HEK293	kidney:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
49	CTCF	chr2:110493714-110494195	HepG2	liver:	n/a	chr2:110493993-110494009 chr2:110493992-110494010 chr2:110493994-110494007 chr2:110493987-110494008
50	CTCF	chr2:110516820-110516852	Medullo	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:110518888-110518938	K562	blood:	n/a
2	chr2:110518888-110518938	A549	lung:	n/a
3	chr2:110518888-110518938	HAEpiC	amniotic membrane:	n/a
4	chr2:110518888-110518938	HCT-116	colon:	n/a
5	chr2:110518888-110518938	HNPCEpiC	eye:	n/a
6	chr2:110518888-110518938	HRCEpiC	kidney:	n/a
7	chr2:110518888-110518938	LNCaP	prostate:	n/a
8	chr2:110518888-110518938	AoSMC	blood vessel:	n/a
9	chr2:110518888-110518938	AG09309	skin:	n/a
10	chr2:110518888-110518938	HCM	heart:	n/a
11	chr2:110518888-110518938	IMR90	lung:	fetal
12	chr2:110518888-110518938	SK-N-MC	brain:	n/a
13	chr2:110518888-110518938	AG09319	gingival:	n/a
14	chr2:110518888-110518938	GM12892	blood:	n/a
15	chr2:110518888-110518938	H1-hESC	embryonic stem cell:	embryo
16	chr2:110518888-110518938	HIPEpiC	eye:	n/a
17	chr2:110518888-110518938	PrEC	prostate:	n/a
18	chr2:110518888-110518938	NHDF-neo	bronchial:	n/a
19	chr2:110518888-110518938	GM12878	blood:	n/a
20	chr2:110518888-110518938	Hepatocyte	liver:	n/a
21	chr2:110518888-110518938	MCF10A-Er-Src	breast:	n/a
22	chr2:110518888-110518938	Caco-2	colon:	n/a
23	chr2:110518888-110518938	SK-N-SH_RA	brain:	n/a
24	chr2:110518888-110518938	HepG2	liver:	n/a
25	chr2:110518888-110518938	NHBE	bronchial:	n/a
26	chr2:110518888-110518938	HEK293	kidney:	embryo
27	chr2:110518888-110518938	CMK	blood:	n/a
28	chr2:110518888-110518938	SAEC	small airway:	n/a
29	chr2:110518888-110518938	AG04449	skin:	fetal
30	chr2:110518888-110518938	HUVEC	blood vessel:	n/a
31	chr2:110518888-110518938	NT2-D1	testis:	n/a
32	chr2:110518888-110518938	BJ	skin:	n/a
33	chr2:110518888-110518938	T-47D	breast:	n/a
34	chr2:110518888-110518938	HRPEpiC	eye:	n/a
35	chr2:110518888-110518938	Hela-S3	cervix:	n/a
36	chr2:110518888-110518938	PFSK-1	brain:	n/a
37	chr2:110518888-110518938	PANC-1	pancreas:	n/a
38	chr2:110518888-110518938	NH-A	brain:	n/a
39	chr2:110518888-110518938	HCF	heart:	n/a
40	chr2:110518888-110518938	HEEpiC	esophagus:	n/a
41	chr2:110518888-110518938	GM12891	blood:	n/a
42	chr2:110518888-110518938	AG10803	skin:	n/a
43	chr2:110518888-110518938	ProgFib	skin:	n/a
44	chr2:110518888-110518938	AG04450	lung:	fetal
45	chr2:110518888-110518938	SK-N-SH	brain:	n/a
46	chr2:110518888-110518938	HCPEpiC	choroid plexus:	n/a
47	chr2:110518888-110518938	NB4	blood:	n/a
48	chr2:110518888-110518938	SKMC	muscle:	n/a
49	chr2:110518888-110518938	RPTEC	kidney:	n/a
50	chr2:110518888-110518938	HPAEpiC	pulmonary alveolar:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGPD5-1	chr2:110490308-110490713	NONHSAT073149

Variant related genes	Relation type
RPL22P11	TF binding region
ENSG00000233307	TF binding region
RPL22P11	CpG island
ENSG00000233307	CpG island
ENSG00000186522	chromatin interactions

Extended variants
information (count: 1019 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1019 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562956490	chr2:110462560-110462561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530589687	chr2:110462589-110462590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371431723	chr2:110462652-110462653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs3066007	chr2:110462680-110462681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545143319	chr2:110462687-110462688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532392674	chr2:110462691-110462692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142590748	chr2:110462728-110462729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533425853	chr2:110462771-110462772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185165885	chr2:110462793-110462794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532950091	chr2:110462795-110462796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546650555	chr2:110462840-110462841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550317909	chr2:110462844-110462845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566750343	chr2:110462907-110462908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150986024	chr2:110462971-110462972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555501430	chr2:110462991-110462992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568966627	chr2:110462993-110462994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538290835	chr2:110463017-110463018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557825102	chr2:110463065-110463066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191110756	chr2:110463089-110463090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115753515	chr2:110463129-110463130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377447414	chr2:110463203-110463204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183211029	chr2:110463228-110463229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140900986	chr2:110463260-110463261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34229733	chr2:110463288-110463289	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531811165	chr2:110463304-110463305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186999601	chr2:110463314-110463315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564156363	chr2:110463358-110463359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372872658	chr2:110463384-110463385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533085954	chr2:110463385-110463386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62151726	chr2:110463422-110463423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559905333	chr2:110463460-110463461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376644301	chr2:110463478-110463479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541568824	chr2:110463509-110463510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529146003	chr2:110463547-110463548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144704376	chr2:110463610-110463611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569178306	chr2:110463619-110463620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537634195	chr2:110463655-110463656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191537512	chr2:110463702-110463703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571380378	chr2:110463732-110463733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534043164	chr2:110463741-110463742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553710375	chr2:110463775-110463776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566290408	chr2:110463785-110463786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146661124	chr2:110463791-110463792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140216455	chr2:110463800-110463801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535329128	chr2:110463811-110463812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11682853	chr2:110463824-110463825	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs576709522	chr2:110463843-110463844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545593358	chr2:110463844-110463845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138303185	chr2:110463942-110463943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183449242	chr2:110464010-110464011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110458800-110463200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:110458800-110468400	Weak transcription	Right Atrium	heart
3	chr2:110460200-110463000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr2:110460200-110463000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:110460200-110464000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:110460200-110468800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:110460200-110469200	Weak transcription	Lung	lung
8	chr2:110460400-110467000	Weak transcription	Stomach Mucosa	stomach
9	chr2:110460600-110465000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:110461000-110467000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr2:110461000-110474200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr2:110461200-110467000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr2:110461400-110464600	Weak transcription	Fetal Lung	lung
14	chr2:110461800-110463000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:110461800-110463000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr2:110462000-110463000	Weak transcription	Hela-S3	cervix
17	chr2:110462000-110463200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr2:110462000-110464400	Weak transcription	Esophagus	oesophagus
19	chr2:110462000-110469000	Weak transcription	HepG2	liver
20	chr2:110463000-110463200	Enhancers	Hela-S3	cervix
21	chr2:110463000-110463400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr2:110463000-110463800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:110463000-110464200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr2:110463000-110464600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:110463200-110464000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr2:110463200-110464200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:110464000-110464200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr2:110464400-110466200	Enhancers	Esophagus	oesophagus
29	chr2:110464600-110468200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:110465000-110465400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:110466200-110473000	Weak transcription	Esophagus	oesophagus
32	chr2:110467000-110467200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr2:110467000-110467200	Enhancers	Stomach Mucosa	stomach
34	chr2:110467000-110467400	Enhancers	Duodenum Mucosa	Duodenum
35	chr2:110467000-110467600	Enhancers	Colonic Mucosa	Colon
36	chr2:110467000-110467600	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr2:110467000-110468600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr2:110467000-110470000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr2:110467200-110468000	Weak transcription	Stomach Mucosa	stomach
40	chr2:110467200-110468200	Weak transcription	Spleen	Spleen
41	chr2:110468000-110468400	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr2:110468000-110468400	Enhancers	Stomach Mucosa	stomach
43	chr2:110468000-110469800	Enhancers	Fetal Heart	heart
44	chr2:110468200-110468400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:110468200-110468600	Enhancers	Spleen	Spleen
46	chr2:110468400-110468800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:110468400-110469600	Enhancers	Right Atrium	heart
48	chr2:110468600-110469600	Enhancers	Right Ventricle	heart
49	chr2:110468600-110472800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr2:110468800-110469200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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