Variant report

Variant	nsv899492
Chromosome Location	chr12:104151560-104183658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:411)
CpG islands
(count:245)
Chromatin interactive
region (count:33)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:104179242-104179647	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:104165372-104165467	HepG2	liver:	n/a	n/a
3	BHLHE40	chr12:104165289-104165416	K562	blood:	n/a	n/a
4	CEBPB	chr12:104174107-104174300	HepG2	liver:	n/a	n/a
5	CEBPB	chr12:104179122-104179394	HepG2	liver:	n/a	chr12:104179214-104179225
6	CEBPB	chr12:104174023-104174310	A549	lung:	n/a	n/a
7	CEBPB	chr12:104179129-104179274	HepG2	liver:	n/a	chr12:104179214-104179225
8	CEBPZ	chr12:104177060-104177079	HepG2	liver:	n/a	n/a
9	CHD2	chr12:104162607-104163022	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr12:104165340-104165490	GM12865	blood:	n/a	n/a
11	CTCF	chr12:104165340-104165490	GM12872	blood:	n/a	n/a
12	CTCF	chr12:104165240-104165390	GM12867	blood:	n/a	n/a
13	CTCF	chr12:104165268-104165492	GM13977	blood:	n/a	n/a
14	CTCF	chr12:104162520-104162670	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr12:104178100-104178250	HEK293	kidney:	n/a	n/a
16	CTCF	chr12:104165030-104165602	IMR90	lung:	n/a	n/a
17	CTCF	chr12:104165320-104165470	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr12:104165320-104165470	RPTEC	kidney:	n/a	n/a
19	CTCF	chr12:104165255-104165533	Fibrobl	skin:	n/a	n/a
20	CTCF	chr12:104165260-104165410	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr12:104165340-104165490	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:104165287-104165525	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr12:104165320-104165470	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr12:104165309-104165513	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr12:104165320-104165470	GM12878	blood:	n/a	n/a
26	CTCF	chr12:104165273-104165508	ProgFib	skin:	n/a	n/a
27	CTCF	chr12:104152740-104152890	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr12:104165365-104165423	GM13976	blood:	n/a	n/a
29	CTCF	chr12:104165255-104165547	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:104152732-104152804	K562	blood:	n/a	n/a
31	CTCF	chr12:104162600-104162750	HMF	breast:	n/a	n/a
32	CTCF	chr12:104165193-104165607	A549	lung:	n/a	n/a
33	CTCF	chr12:104165280-104165430	HCT-116	colon:	n/a	n/a
34	CTCF	chr12:104165294-104165514	GM19238	blood:	n/a	n/a
35	CTCF	chr12:104165420-104165570	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr12:104165340-104165490	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr12:104178211-104178352	GM12878	blood:	n/a	n/a
38	CTCF	chr12:104162620-104162770	AG09319	gingival:	n/a	n/a
39	CTCF	chr12:104165320-104165470	HRE	kidney:	n/a	n/a
40	CTCF	chr12:104178178-104178378	NHEK	skin:	n/a	n/a
41	CTCF	chr12:104162613-104162703	K562	blood:	n/a	n/a
42	CTCF	chr12:104165280-104165430	GM12871	blood:	n/a	n/a
43	CTCF	chr12:104162640-104162790	NB4	blood:	n/a	n/a
44	CTCF	chr12:104165320-104165470	GM12872	blood:	n/a	n/a
45	CTCF	chr12:104165340-104165490	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr12:104165260-104165410	GM12870	blood:	n/a	n/a
47	CTCF	chr12:104165320-104165470	HVMF	connective:	n/a	n/a
48	CTCF	chr12:104165320-104165470	GM06990	blood:	n/a	n/a
49	CTCF	chr12:104165360-104165510	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr12:104162628-104162748	MCF-7	breast:	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	chr12:104173675-104173725	HRCEpiC	kidney:	n/a
2	chr12:104173675-104173725	HRCEpiC	kidney:	n/a
3	chr12:104178138-104178188	SK-N-MC	brain:	n/a
4	chr12:104166357-104166407	HCPEpiC	choroid plexus:	n/a
5	chr12:104166357-104166407	HIPEpiC	eye:	n/a
6	chr12:104163467-104163517	ProgFib	skin:	n/a
7	chr12:104178138-104178188	Hela-S3	cervix:	n/a
8	chr12:104178138-104178188	HCF	heart:	n/a
9	chr12:104163467-104163517	HEEpiC	esophagus:	n/a
10	chr12:104166357-104166407	AG09319	gingival:	n/a
11	chr12:104173675-104173725	HCPEpiC	choroid plexus:	n/a
12	chr12:104178138-104178188	AG04450	lung:	fetal
13	chr12:104163467-104163517	NHBE	bronchial:	n/a
14	chr12:104163467-104163517	T-47D	breast:	n/a
15	chr12:104166357-104166407	PANC-1	pancreas:	n/a
16	chr12:104163467-104163517	HCM	heart:	n/a
17	chr12:104163467-104163517	AG09319	gingival:	n/a
18	chr12:104178138-104178188	AG04449	skin:	fetal
19	chr12:104166357-104166407	K562	blood:	n/a
20	chr12:104178138-104178188	Caco-2	colon:	n/a
21	chr12:104173675-104173725	AG04449	skin:	fetal
22	chr12:104173675-104173725	CMK	blood:	n/a
23	chr12:104173675-104173725	HNPCEpiC	eye:	n/a
24	chr12:104173675-104173725	A549	lung:	n/a
25	chr12:104166357-104166407	H1-hESC	embryonic stem cell:	embryo
26	chr12:104178138-104178188	SK-N-SH	brain:	n/a
27	chr12:104166357-104166407	HCM	heart:	n/a
28	chr12:104163467-104163517	HNPCEpiC	eye:	n/a
29	chr12:104178138-104178188	Jurkat	blood:	n/a
30	chr12:104166357-104166407	HUVEC	blood vessel:	n/a
31	chr12:104173675-104173725	BE2_C	brain:	n/a
32	chr12:104163467-104163517	NHDF-neo	bronchial:	n/a
33	chr12:104163467-104163517	AG04449	skin:	fetal
34	chr12:104173675-104173725	PFSK-1	brain:	n/a
35	chr12:104166357-104166407	ovcar-3	ovarian:	n/a
36	chr12:104178138-104178188	HNPCEpiC	eye:	n/a
37	chr12:104163467-104163517	H1-hESC	embryonic stem cell:	embryo
38	chr12:104173675-104173725	ovcar-3	ovarian:	n/a
39	chr12:104163467-104163517	HRPEpiC	eye:	n/a
40	chr12:104173675-104173725	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:104166357-104166407	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:104178138-104178188	HMEC	breast:	n/a
43	chr12:104173675-104173725	SK-N-MC	brain:	n/a
44	chr12:104163467-104163517	SAEC	small airway:	n/a
45	chr12:104178138-104178188	NT2-D1	testis:	n/a
46	chr12:104163467-104163517	ECC-1	luminal epithelium:	n/a
47	chr12:104163467-104163517	PFSK-1	brain:	n/a
48	chr12:104163467-104163517	HCT-116	colon:	n/a
49	chr12:104178138-104178188	NB4	blood:	n/a
50	chr12:104173675-104173725	HEK293	kidney:	embryo

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:104156225..104158975-chr12:104165385..104167206,2	MCF-7	breast:
2	chr12:104178636..104180567-chr12:104180995..104183516,2	K562	blood:
3	chr12:104164135..104167659-chr12:104253252..104255970,3	MCF-7	breast:
4	chr12:104160749..104162806-chr12:104234443..104236279,2	MCF-7	breast:
5	chr12:104166261..104169463-chr12:104174698..104177836,3	MCF-7	breast:
6	chr12:104141190..104143680-chr12:104152511..104154434,2	MCF-7	breast:
7	chr12:104164150..104167607-chr12:104233925..104237712,5	MCF-7	breast:
8	chr12:104168330..104170721-chr12:104177797..104180026,2	MCF-7	breast:
9	chr12:104166229..104169114-chr12:104169303..104172896,3	MCF-7	breast:
10	chr12:104164880..104166150-chr12:104263725..104264827,7	MCF-7	breast:
11	chr12:104177175..104180567-chr12:104180842..104183516,3	K562	blood:
12	chr12:104165257..104167122-chr12:104234296..104237264,2	MCF-7	breast:
13	chr12:104164872..104166111-chr12:104264007..104265181,16	MCF-7	breast:
14	chr12:104167428..104170420-chr12:104235158..104237169,3	K562	blood:
15	chr12:104163154..104166859-chr12:104341815..104344175,3	K562	blood:
16	chr12:104156601..104158304-chr12:104234434..104236510,2	MCF-7	breast:
17	chr12:104168307..104171120-chr12:104193442..104196343,2	K562	blood:
18	chr12:104163207..104165311-chr12:104196733..104198239,2	K562	blood:
19	chr12:104165050..104165668-chr12:104234645..104235407,2	MCF-7	breast:
20	chr12:104176398..104178432-chr12:104233589..104235807,2	MCF-7	breast:
21	chr12:104152829..104155541-chr12:104264505..104266459,2	MCF-7	breast:
22	chr12:104177175..104180567-chr12:104180842..104183516,3	K562	blood:
23	chr12:104171358..104174943-chr12:104233480..104236232,4	MCF-7	breast:
24	chr12:104026135..104027046-chr12:104165031..104165600,2	MCF-7	breast:
25	chr12:104178670..104180428-chr12:104186156..104188204,2	K562	blood:
26	chr12:104156978..104159954-chr12:104162925..104164742,3	MCF-7	breast:
27	chr12:104136425..104139178-chr12:104152624..104154639,2	K562	blood:
28	chr12:104026112..104026905-chr12:104163740..104164680,2	MCF-7	breast:
29	chr12:104163986..104166339-chr12:104260477..104262512,3	MCF-7	breast:
30	chr12:104178636..104180567-chr12:104180995..104183516,2	K562	blood:
31	chr12:104166261..104169463-chr12:104174698..104177836,3	MCF-7	breast:
32	chr12:104181732..104183493-chr12:104185105..104187662,2	K562	blood:
33	chr12:104166229..104169114-chr12:104169303..104172896,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NT5DC3-1	chr12:104160513-104160684	ENSG00000257681.1
2	lnc-NT5DC3-1	chr12:104160513-104160691	ENSG00000257681.1
3	lnc-NT5DC3-1	chr12:104162585-104162636	ENSG00000257681.1
4	lnc-NT5DC3-1	chr12:104157090-104157596	ENSG00000257681.1

No data

Variant related genes	Relation type
STAB2	TF binding region
NT5DC3	TF binding region
ENSG00000257681	TF binding region
STAB2	CpG island
NT5DC3	CpG island
ENSG00000257681	CpG island
ENSG00000111696	chromatin interactions
ENSG00000257327	chromatin interactions
ENSG00000136011	chromatin interactions

Extended variants
information (count: 1361 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11834389	chr12:104151560-104151561	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34393550	chr12:104151593-104151594	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs55766192	chr12:104151601-104151602	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs544126152	chr12:104151612-104151613	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs56863355	chr12:104151678-104151679	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs138070557	chr12:104151710-104151711	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545340064	chr12:104151721-104151722	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113503423	chr12:104151733-104151734	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559741598	chr12:104151736-104151737	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147446641	chr12:104151797-104151798	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10861091	chr12:104151798-104151799	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563082771	chr12:104151825-104151826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532020616	chr12:104151876-104151877	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530788328	chr12:104151879-104151880	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374883001	chr12:104151903-104151904	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370589581	chr12:104151909-104151910	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs199904116	chr12:104151921-104151922	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112677985	chr12:104151926-104151927	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12425537	chr12:104151931-104151932	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs142853959	chr12:104151979-104151980	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534056039	chr12:104151984-104151985	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs151063567	chr12:104151985-104151986	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375356533	chr12:104152022-104152023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368930302	chr12:104152087-104152088	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570869001	chr12:104152094-104152095	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567644160	chr12:104152127-104152128	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs58956630	chr12:104152131-104152132	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs556595835	chr12:104152187-104152188	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575491680	chr12:104152198-104152199	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs193022982	chr12:104152213-104152214	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs3834932	chr12:104152227-104152228	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554498277	chr12:104152228-104152229	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574549147	chr12:104152260-104152261	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546392295	chr12:104152273-104152274	Enhancers Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184664323	chr12:104152280-104152281	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs3763993	chr12:104152283-104152284	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs576523072	chr12:104152303-104152304	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs538643442	chr12:104152335-104152336	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs568980985	chr12:104152351-104152352	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538002456	chr12:104152352-104152353	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs562485032	chr12:104152365-104152366	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs138334594	chr12:104152384-104152385	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs548830239	chr12:104152386-104152387	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs556947795	chr12:104152396-104152397	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs4981026	chr12:104152456-104152457	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs547921519	chr12:104152477-104152478	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs143911941	chr12:104152485-104152486	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs568784444	chr12:104152517-104152518	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs554788442	chr12:104152540-104152541	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs533460574	chr12:104152547-104152548	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104139200-104154200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr12:104140600-104154600	Weak transcription	Aorta	Aorta
3	chr12:104142600-104152200	Weak transcription	HMEC	breast
4	chr12:104142800-104152000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:104142800-104154600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:104142800-104154600	Weak transcription	NHEK	skin
7	chr12:104145600-104154800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr12:104145800-104152000	Weak transcription	HSMMtube	muscle
9	chr12:104145800-104152400	Weak transcription	Esophagus	oesophagus
10	chr12:104145800-104166800	Weak transcription	Right Atrium	heart
11	chr12:104146000-104154600	Weak transcription	HSMM	muscle
12	chr12:104146200-104169400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:104147000-104152200	Strong transcription	Spleen	Spleen
14	chr12:104147000-104159600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr12:104147000-104165400	Strong transcription	Stomach Smooth Muscle	stomach
16	chr12:104147400-104155800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:104148000-104154200	Weak transcription	Colon Smooth Muscle	Colon
18	chr12:104148200-104154400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr12:104148800-104152200	Weak transcription	Gastric	stomach
20	chr12:104149000-104156800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr12:104149200-104154200	Weak transcription	A549	lung
22	chr12:104149400-104152200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr12:104149600-104153800	Weak transcription	Liver	Liver
24	chr12:104150000-104156600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr12:104150000-104166800	Weak transcription	Brain Cingulate Gyrus	brain
26	chr12:104150600-104151600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr12:104150600-104154200	Weak transcription	Placenta	Placenta
28	chr12:104150600-104155200	Weak transcription	Fetal Intestine Small	intestine
29	chr12:104151200-104153000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr12:104151200-104153200	Strong transcription	Fetal Stomach	stomach
31	chr12:104151400-104152600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr12:104151400-104152800	Enhancers	Fetal Muscle Trunk	muscle
33	chr12:104151400-104154800	Weak transcription	NH-A	brain
34	chr12:104151400-104158000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:104151600-104152200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr12:104151600-104152800	Enhancers	Fetal Muscle Leg	muscle
37	chr12:104151600-104152800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr12:104151600-104155000	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr12:104151600-104170400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr12:104151800-104152000	Enhancers	Lung	lung
41	chr12:104151800-104152600	Enhancers	Psoas Muscle	Psoas
42	chr12:104151800-104154800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr12:104152000-104152200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr12:104152000-104152400	Enhancers	HSMMtube	muscle
45	chr12:104152000-104152800	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr12:104152000-104159800	Weak transcription	Lung	lung
47	chr12:104152200-104152400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr12:104152200-104152400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr12:104152200-104152400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr12:104152200-104152400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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