Variant report

Variant	nsv648
Chromosome Location	chr12:26330291-26375186
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:396)
CpG islands
(count:1038)
Chromatin interactive
region (count:12)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:26348752-26349149	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr12:26341185-26341486	GM12878	blood:	n/a	chr12:26341364-26341375
3	BATF	chr12:26330224-26330567	GM12878	blood:	n/a	chr12:26330444-26330454
4	BATF	chr12:26330306-26330574	GM12878	blood:	n/a	chr12:26330444-26330454
5	BCL3	chr12:26338513-26338759	GM12878	blood:	n/a	n/a
6	CEBPB	chr12:26366302-26366353	HepG2	liver:	n/a	n/a
7	CEBPB	chr12:26345150-26345408	HepG2	liver:	n/a	chr12:26345263-26345274
8	CHD1	chr12:26348752-26348870	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr12:26346502-26346599	GM12878	blood:	n/a	n/a
10	CHD2	chr12:26348750-26349015	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr12:26348711-26349438	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr12:26368381-26368463	Fibrobl	skin:	n/a	n/a
13	CTCF	chr12:26340518-26340609	H1-hESC	embryonic stem cell:	n/a	chr12:26340570-26340578
14	CTCF	chr12:26340440-26340590	SK-N-SH_RA	brain:	n/a	chr12:26340570-26340578
15	CTCF	chr12:26340520-26340670	Caco-2	colon:	n/a	chr12:26340649-26340670 chr12:26340570-26340578
16	CTCF	chr12:26349020-26349170	HPF	lung:	n/a	n/a
17	CTCF	chr12:26340480-26340630	HCPEpiC	choroid plexus:	n/a	chr12:26340570-26340578
18	CTCF	chr12:26348760-26348910	HAc	cerebellar:	n/a	n/a
19	CTCF	chr12:26340500-26340650	GM12875	blood:	n/a	chr12:26340570-26340578
20	CTCF	chr12:26340540-26340690	GM12875	blood:	n/a	chr12:26340649-26340670 chr12:26340570-26340578
21	CTCF	chr12:26349084-26349152	GM12878	blood:	n/a	n/a
22	CTCF	chr12:26340510-26340637	GM19239	blood:	n/a	chr12:26340570-26340578
23	CTCF	chr12:26340520-26340616	Pancreas_OC	pancreas:	n/a	chr12:26340570-26340578
24	CTCF	chr12:26340516-26340614	GM19240	blood:	n/a	chr12:26340570-26340578
25	CTCF	chr12:26332380-26332530	HEK293	kidney:	n/a	n/a
26	CTCF	chr12:26340540-26340690	AG04449	skin:	n/a	chr12:26340649-26340670 chr12:26340570-26340578
27	CTCF	chr12:26340500-26340650	HMF	breast:	n/a	chr12:26340570-26340578
28	CTCF	chr12:26340520-26340670	GM12871	blood:	n/a	chr12:26340649-26340670 chr12:26340570-26340578
29	CTCF	chr12:26337740-26337890	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr12:26340524-26340613	NHEK	skin:	n/a	chr12:26340570-26340578
31	CTCF	chr12:26349069-26349097	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:26340460-26340610	HMF	breast:	n/a	chr12:26340570-26340578
33	CTCF	chr12:26340484-26340665	GM12878	blood:	n/a	chr12:26340570-26340578
34	CTCF	chr12:26340500-26340650	HRPEpiC	eye:	n/a	chr12:26340570-26340578
35	CTCF	chr12:26340480-26340630	GM12871	blood:	n/a	chr12:26340570-26340578
36	CTCF	chr12:26340440-26340590	AG09319	gingival:	n/a	chr12:26340570-26340578
37	CTCF	chr12:26340500-26340650	HCT-116	colon:	n/a	chr12:26340570-26340578
38	CTCF	chr12:26349076-26349178	ProgFib	skin:	n/a	n/a
39	CTCF	chr12:26340520-26340670	NB4	blood:	n/a	chr12:26340649-26340670 chr12:26340570-26340578
40	CTCF	chr12:26340480-26340630	HepG2	liver:	n/a	chr12:26340570-26340578
41	CTCF	chr12:26349020-26349170	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr12:26340520-26340670	GM12874	blood:	n/a	chr12:26340649-26340670 chr12:26340570-26340578
43	CTCF	chr12:26348980-26349130	RPTEC	kidney:	n/a	n/a
44	CTCF	chr12:26340512-26340653	GM13977	blood:	n/a	chr12:26340570-26340578
45	CTCF	chr12:26349092-26349133	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:26349040-26349190	AG09319	gingival:	n/a	n/a
47	CTCF	chr12:26340520-26340670	MCF-7	breast:	n/a	chr12:26340649-26340670 chr12:26340570-26340578
48	CTCF	chr12:26340480-26340630	HAc	cerebellar:	n/a	chr12:26340570-26340578
49	CTCF	chr12:26340540-26340690	GM12873	blood:	n/a	chr12:26340649-26340670 chr12:26340570-26340578
50	CTCF	chr12:26332400-26332550	HAc	cerebellar:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:26349002-26349052	HEEpiC	esophagus:	n/a
2	chr12:26349002-26349052	HEEpiC	esophagus:	n/a
3	chr12:26347100-26347150	H1-hESC	embryonic stem cell:	embryo
4	chr12:26348331-26348381	SAEC	small airway:	n/a
5	chr12:26348343-26348393	NHBE	bronchial:	n/a
6	chr12:26345227-26345277	HRCEpiC	kidney:	n/a
7	chr12:26349469-26349519	HCF	heart:	n/a
8	chr12:26347596-26347646	MCF10A-Er-Src	breast:	n/a
9	chr12:26340863-26340913	MCF-7	breast:	n/a
10	chr12:26348333-26348383	HRCEpiC	kidney:	n/a
11	chr12:26348529-26348579	AG10803	skin:	n/a
12	chr12:26348343-26348393	MCF10A-Er-Src	breast:	n/a
13	chr12:26348463-26348513	AG04450	lung:	fetal
14	chr12:26348343-26348393	HUVEC	blood vessel:	n/a
15	chr12:26348463-26348513	CMK	blood:	n/a
16	chr12:26348343-26348393	GM06990	blood:	n/a
17	chr12:26348463-26348513	MCF10A-Er-Src	breast:	n/a
18	chr12:26348093-26348143	AG09319	gingival:	n/a
19	chr12:26340863-26340913	A549	lung:	n/a
20	chr12:26348331-26348381	NB4	blood:	n/a
21	chr12:26351840-26351890	CMK	blood:	n/a
22	chr12:26347100-26347150	T-47D	breast:	n/a
23	chr12:26349469-26349519	RPTEC	kidney:	n/a
24	chr12:26347596-26347646	HepG2	liver:	n/a
25	chr12:26349469-26349519	PFSK-1	brain:	n/a
26	chr12:26345227-26345277	SK-N-SH	brain:	n/a
27	chr12:26348437-26348487	Caco-2	colon:	n/a
28	chr12:26348463-26348513	GM12878	blood:	n/a
29	chr12:26349469-26349519	BJ	skin:	n/a
30	chr12:26348437-26348487	CMK	blood:	n/a
31	chr12:26345227-26345277	GM19239	blood:	n/a
32	chr12:26348331-26348381	AG10803	skin:	n/a
33	chr12:26349002-26349052	AG09319	gingival:	n/a
34	chr12:26347596-26347646	HCF	heart:	n/a
35	chr12:26349469-26349519	GM12878	blood:	n/a
36	chr12:26347100-26347150	BJ	skin:	n/a
37	chr12:26348117-26348167	Hela-S3	cervix:	n/a
38	chr12:26340863-26340913	HCM	heart:	n/a
39	chr12:26349129-26349179	HMEC	breast:	n/a
40	chr12:26349469-26349519	SK-N-SH_RA	brain:	n/a
41	chr12:26348093-26348143	Hela-S3	cervix:	n/a
42	chr12:26348117-26348167	K562	blood:	n/a
43	chr12:26348343-26348393	Caco-2	colon:	n/a
44	chr12:26340863-26340913	NHBE	bronchial:	n/a
45	chr12:26349129-26349179	HEK293	kidney:	embryo
46	chr12:26349129-26349179	HRPEpiC	eye:	n/a
47	chr12:26340863-26340913	SK-N-SH_RA	brain:	n/a
48	chr12:26347100-26347150	HepG2	liver:	n/a
49	chr12:26348117-26348167	HCF	heart:	n/a
50	chr12:26349129-26349179	HRE	kidney:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:26340066..26341948-chr12:26347429..26349179,2	MCF-7	breast:
2	chr12:26372294..26374868-chr12:26375069..26377161,2	MCF-7	breast:
3	chr12:26372294..26374868-chr12:26375069..26377161,2	MCF-7	breast:
4	chr12:26326842..26329706-chr12:26330905..26334715,3	K562	blood:
5	chr12:26340370..26340991-chr12:26427254..26427993,2	MCF-7	breast:
6	chr12:26340413..26342311-chr12:26359943..26362244,2	K562	blood:
7	chr12:26357801..26359384-chr12:26374632..26376428,2	K562	blood:
8	chr12:26351932..26353436-chr12:26357817..26360004,2	MCF-7	breast:
9	chr12:26308693..26311647-chr12:26329505..26331946,2	K562	blood:
10	chr12:26340413..26342311-chr12:26359943..26362244,2	K562	blood:
11	chr12:26357801..26359384-chr12:26374632..26376428,2	K562	blood:
12	chr12:26351932..26353436-chr12:26357817..26360004,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITPR2-3	chr12:26367650-26367710	ENSG00000256234.1
2	lnc-SSPN-3	chr12:26348160-26348546	l_621_chr12:26342464-26348546_testes
3	lnc-SSPN-3	chr12:26347810-26348109	l_621_chr12:26342464-26348546_testes
4	lnc-SSPN-3	chr12:26348289-26348464	NONHSAT027395
5	lnc-RASSF8-1	chr12:26332929-26334217	NONHSAT027394
6	lnc-SSPN-3	chr12:26342465-26342625	l_621_chr12:26342464-26348546_testes
7	lnc-SSPN-3	chr12:26343426-26343463	l_621_chr12:26342464-26348546_testes
8	lnc-ITPR2-3	chr12:26364097-26364604	ENSG00000256234.1
9	lnc-RASSF8-1	chr12:26332929-26334216	XLOC_009692

No data

Variant related genes	Relation type
SSPN	TF binding region
SSPN	CpG island
ENSG00000123096	chromatin interactions

Extended variants
information (count: 1492 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1492 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553748122	chr12:26330302-26330303	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs138010144	chr12:26330322-26330323	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs116910287	chr12:26330330-26330331	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs1466467	chr12:26330372-26330373	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs80152952	chr12:26330420-26330421	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs543569340	chr12:26330468-26330469	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs1466466	chr12:26330469-26330470	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs532390139	chr12:26330487-26330488	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs192079429	chr12:26330493-26330494	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs1466465	chr12:26330500-26330501	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs182868538	chr12:26330537-26330538	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs529626819	chr12:26330571-26330572	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs547812590	chr12:26330599-26330600	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs569708041	chr12:26330620-26330621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187932230	chr12:26330628-26330629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112358148	chr12:26330662-26330663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140741936	chr12:26330669-26330670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535669713	chr12:26330722-26330723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192408394	chr12:26330766-26330767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17380416	chr12:26330797-26330798	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs553684881	chr12:26330820-26330821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114786819	chr12:26330821-26330822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535821087	chr12:26330864-26330865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557406073	chr12:26330871-26330872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527283702	chr12:26330891-26330892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2343868	chr12:26330940-26330941	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs182380410	chr12:26331021-26331022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61914464	chr12:26331026-26331027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534418720	chr12:26331130-26331131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74072076	chr12:26331133-26331134	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs768347	chr12:26331146-26331147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs544933450	chr12:26331147-26331148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140845734	chr12:26331201-26331202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529962274	chr12:26331202-26331203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368627652	chr12:26331222-26331223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541394024	chr12:26331280-26331281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527338818	chr12:26331288-26331289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374225939	chr12:26331289-26331290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563149479	chr12:26331296-26331297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373576841	chr12:26331297-26331298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530583343	chr12:26331298-26331299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187991187	chr12:26331306-26331307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369535840	chr12:26331331-26331332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192262013	chr12:26331335-26331336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185054841	chr12:26331348-26331349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532913750	chr12:26331402-26331403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547234457	chr12:26331470-26331471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372946393	chr12:26331480-26331481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200601756	chr12:26331493-26331494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150426217	chr12:26331522-26331523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
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
Testicular germ cell tumor	18059402	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	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Hepatocellular carcinoma	16750200	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26328200-26331200	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr12:26329200-26331000	Enhancers	Fetal Intestine Small	intestine
3	chr12:26329200-26331200	Enhancers	Fetal Intestine Large	intestine
4	chr12:26329400-26330600	Enhancers	Stomach Mucosa	stomach
5	chr12:26329400-26331200	Enhancers	Small Intestine	intestine
6	chr12:26329800-26331000	Enhancers	Duodenum Mucosa	Duodenum
7	chr12:26330200-26330400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
8	chr12:26330200-26330600	Enhancers	GM12878-XiMat	blood
9	chr12:26330200-26330600	Enhancers	HMEC	breast
10	chr12:26330200-26330800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:26330400-26330600	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr12:26330400-26330800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr12:26330400-26330800	Enhancers	NHEK	skin
14	chr12:26330600-26330800	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr12:26330600-26331400	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr12:26330600-26332400	Weak transcription	Stomach Mucosa	stomach
17	chr12:26330800-26337800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:26331200-26332400	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr12:26331400-26331800	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr12:26331800-26332400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr12:26332000-26332200	Enhancers	Esophagus	oesophagus
22	chr12:26332200-26332400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr12:26332400-26333400	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr12:26332400-26338200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:26332600-26332800	Enhancers	Stomach Mucosa	stomach
26	chr12:26333200-26333400	Bivalent Enhancer	A549	lung
27	chr12:26334200-26334800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr12:26335800-26336000	Enhancers	Placenta	Placenta
29	chr12:26336000-26336600	Weak transcription	Placenta	Placenta
30	chr12:26336200-26338600	Weak transcription	Psoas Muscle	Psoas
31	chr12:26336600-26337200	Enhancers	Placenta	Placenta
32	chr12:26337000-26337200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:26337200-26338400	Weak transcription	Placenta	Placenta
34	chr12:26337400-26338600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:26337800-26341800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:26338000-26338400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:26338000-26341800	Enhancers	HMEC	breast
38	chr12:26338200-26338400	Enhancers	H9 Cell Line	embryonic stem cell
39	chr12:26338200-26338800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:26338200-26338800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr12:26338200-26339000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:26338200-26341800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:26338200-26341800	Enhancers	NHEK	skin
44	chr12:26338400-26338800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr12:26338400-26338800	Enhancers	Placenta	Placenta
46	chr12:26338400-26338800	Enhancers	NH-A	brain
47	chr12:26338400-26340200	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr12:26338400-26341800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr12:26338400-26341800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr12:26338600-26338800	Enhancers	HSMM	muscle

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