Variant report

Variant	esv1831348
Chromosome Location	chr18:29205526-29268786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1838)
CpG islands
(count:610)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1838 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29206509-29206566	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29227351-29227651	HepG2	liver:	n/a	n/a
3	ATF1	chr18:29213446-29213964	K562	blood:	n/a	n/a
4	ATF1	chr18:29263987-29264156	K562	blood:	n/a	n/a
5	ATF1	chr18:29228931-29229286	K562	blood:	n/a	n/a
6	ATF1	chr18:29222326-29222412	K562	blood:	n/a	n/a
7	ATF1	chr18:29238101-29238424	K562	blood:	n/a	n/a
8	ATF1	chr18:29238852-29239148	K562	blood:	n/a	n/a
9	ATF2	chr18:29228784-29229366	GM12878	blood:	n/a	n/a
10	ATF2	chr18:29237694-29239617	GM12878	blood:	n/a	n/a
11	ATF2	chr18:29214140-29215014	GM12878	blood:	n/a	n/a
12	ATF2	chr18:29229695-29230492	GM12878	blood:	n/a	n/a
13	ATF2	chr18:29214171-29214704	GM12878	blood:	n/a	n/a
14	ATF2	chr18:29233146-29233882	GM12878	blood:	n/a	n/a
15	ATF2	chr18:29228730-29229349	GM12878	blood:	n/a	n/a
16	ATF2	chr18:29226069-29226812	GM12878	blood:	n/a	n/a
17	ATF2	chr18:29265483-29266189	GM12878	blood:	n/a	n/a
18	ATF2	chr18:29232002-29232796	GM12878	blood:	n/a	n/a
19	ATF2	chr18:29237893-29239453	GM12878	blood:	n/a	n/a
20	ATF2	chr18:29210419-29210904	GM12878	blood:	n/a	n/a
21	ATF2	chr18:29226017-29227024	GM12878	blood:	n/a	n/a
22	ATF3	chr18:29228930-29229196	K562	blood:	n/a	n/a
23	BACH1	chr18:29264840-29264850	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr18:29210947-29210976	K562	blood:	n/a	n/a
25	BACH1	chr18:29253684-29253730	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr18:29265299-29265942	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr18:29226310-29226696	GM12878	blood:	n/a	n/a
28	BATF	chr18:29228871-29229273	GM12878	blood:	n/a	chr18:29229096-29229107 chr18:29229097-29229107 chr18:29229126-29229135
29	BATF	chr18:29229774-29230257	GM12878	blood:	n/a	chr18:29230006-29230015
30	BATF	chr18:29214259-29214624	GM12878	blood:	n/a	n/a
31	BATF	chr18:29238187-29239273	GM12878	blood:	n/a	n/a
32	BATF	chr18:29238824-29239246	GM12878	blood:	n/a	n/a
33	BATF	chr18:29229845-29230196	GM12878	blood:	n/a	chr18:29230006-29230015
34	BATF	chr18:29228835-29229291	GM12878	blood:	n/a	chr18:29229096-29229107 chr18:29229097-29229107 chr18:29229126-29229135
35	BATF	chr18:29238232-29238754	GM12878	blood:	n/a	n/a
36	BCL11A	chr18:29238124-29239144	GM12878	blood:	n/a	chr18:29239109-29239118
37	BCL11A	chr18:29228834-29229210	GM12878	blood:	n/a	chr18:29229099-29229108 chr18:29229100-29229109
38	BCL11A	chr18:29228837-29229205	GM12878	blood:	n/a	chr18:29229099-29229108 chr18:29229100-29229109
39	BCL11A	chr18:29238097-29239251	GM12878	blood:	n/a	chr18:29239218-29239227 chr18:29239109-29239118
40	BCL11A	chr18:29229869-29230145	GM12878	blood:	n/a	n/a
41	BCL11A	chr18:29229755-29230256	GM12878	blood:	n/a	n/a
42	BCL3	chr18:29238073-29239294	GM12878	blood:	n/a	chr18:29239218-29239227 chr18:29239109-29239118
43	BCL3	chr18:29238221-29238605	GM12878	blood:	n/a	n/a
44	BCL3	chr18:29228859-29229221	A549	lung:	n/a	chr18:29229099-29229108 chr18:29229100-29229109
45	BCL3	chr18:29228862-29229231	GM12878	blood:	n/a	chr18:29229099-29229108 chr18:29229100-29229109
46	BCL3	chr18:29210486-29210822	GM12878	blood:	n/a	n/a
47	BCL3	chr18:29265013-29265618	GM12878	blood:	n/a	chr18:29265139-29265152 chr18:29265437-29265450 chr18:29265359-29265368 chr18:29265348-29265357
48	BCL3	chr18:29214240-29214705	GM12878	blood:	n/a	n/a
49	BCLAF1	chr18:29264660-29265486	GM12878	blood:	n/a	chr18:29265139-29265152 chr18:29264714-29264727 chr18:29265437-29265450 chr18:29265359-29265368 chr18:29264766-29264779 chr18:29265348-29265357
50	BCLAF1	chr18:29238004-29239516	GM12878	blood:	n/a	chr18:29239218-29239227 chr18:29239109-29239118

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29265840-29265890	NB4	blood:	n/a
2	chr18:29265840-29265890	HRPEpiC	eye:	n/a
3	chr18:29263741-29263791	RPTEC	kidney:	n/a
4	chr18:29262121-29262171	PANC-1	pancreas:	n/a
5	chr18:29264051-29264101	HCT-116	colon:	n/a
6	chr18:29268737-29268787	MCF10A-Er-Src	breast:	n/a
7	chr18:29264051-29264101	IMR90	lung:	fetal
8	chr18:29264051-29264101	HRCEpiC	kidney:	n/a
9	chr18:29265840-29265890	SK-N-MC	brain:	n/a
10	chr18:29258797-29258847	HUVEC	blood vessel:	n/a
11	chr18:29264431-29264481	MCF-7	breast:	n/a
12	chr18:29265840-29265890	HCPEpiC	choroid plexus:	n/a
13	chr18:29265842-29265892	GM12892	blood:	n/a
14	chr18:29264051-29264101	NHDF-neo	bronchial:	n/a
15	chr18:29264252-29264302	HPAEpiC	pulmonary alveolar:	n/a
16	chr18:29264252-29264302	Hepatocyte	liver:	n/a
17	chr18:29258797-29258847	Jurkat	blood:	n/a
18	chr18:29262121-29262171	HAEpiC	amniotic membrane:	n/a
19	chr18:29268737-29268787	SK-N-SH_RA	brain:	n/a
20	chr18:29258797-29258847	NB4	blood:	n/a
21	chr18:29268737-29268787	HEEpiC	esophagus:	n/a
22	chr18:29265487-29265537	GM12891	blood:	n/a
23	chr18:29265840-29265890	HPAEpiC	pulmonary alveolar:	n/a
24	chr18:29264431-29264481	Hepatocyte	liver:	n/a
25	chr18:29264051-29264101	BE2_C	brain:	n/a
26	chr18:29265840-29265890	PANC-1	pancreas:	n/a
27	chr18:29268737-29268787	GM12878	blood:	n/a
28	chr18:29265840-29265890	HCF	heart:	n/a
29	chr18:29262121-29262171	HPAEpiC	pulmonary alveolar:	n/a
30	chr18:29265840-29265890	K562	blood:	n/a
31	chr18:29264252-29264302	ProgFib	skin:	n/a
32	chr18:29262121-29262171	Jurkat	blood:	n/a
33	chr18:29264051-29264101	BJ	skin:	n/a
34	chr18:29265840-29265890	GM19239	blood:	n/a
35	chr18:29265842-29265892	HIPEpiC	eye:	n/a
36	chr18:29263741-29263791	H1-hESC	embryonic stem cell:	embryo
37	chr18:29262121-29262171	HepG2	liver:	n/a
38	chr18:29262121-29262171	HEEpiC	esophagus:	n/a
39	chr18:29264431-29264481	NT2-D1	testis:	n/a
40	chr18:29265842-29265892	SK-N-MC	brain:	n/a
41	chr18:29264252-29264302	RPTEC	kidney:	n/a
42	chr18:29265487-29265537	LNCaP	prostate:	n/a
43	chr18:29264252-29264302	LNCaP	prostate:	n/a
44	chr18:29264431-29264481	HCPEpiC	choroid plexus:	n/a
45	chr18:29265487-29265537	HNPCEpiC	eye:	n/a
46	chr18:29265840-29265890	NT2-D1	testis:	n/a
47	chr18:29264252-29264302	GM06990	blood:	n/a
48	chr18:29262121-29262171	AG09309	skin:	n/a
49	chr18:29263741-29263791	Caco-2	colon:	n/a
50	chr18:29263741-29263791	GM12892	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29266991..29268512-chr18:29271793..29273586,2	K562	blood:
2	chr18:29209445..29212073-chr18:29221671..29224174,2	K562	blood:
3	chr18:29219249..29221553-chr18:29225572..29227383,2	MCF-7	breast:
4	chr18:29259339..29260872-chr18:29261230..29264110,2	K562	blood:
5	chr17:56708485..56709372-chr18:29264759..29265403,2	Hela-S3	cervix:
6	chr18:29259339..29260872-chr18:29261230..29264110,2	K562	blood:
7	chr18:29235239..29238459-chr18:29263541..29266170,4	MCF-7	breast:
8	chr18:29235060..29236900-chr18:29250262..29252488,2	MCF-7	breast:
9	chr18:29251332..29253649-chr18:29260084..29261711,2	K562	blood:
10	chr18:29135623..29136433-chr18:29206170..29207050,3	MCF-7	breast:
11	chr18:29251332..29253649-chr18:29260084..29261711,2	K562	blood:
12	chr18:29219456..29221928-chr18:29224647..29227313,2	K562	blood:
13	chr18:29219249..29221553-chr18:29225572..29227383,2	MCF-7	breast:
14	chr18:29257336..29259422-chr18:29266158..29267928,2	K562	blood:
15	chr18:29145542..29146264-chr18:29205706..29207014,3	MCF-7	breast:
16	chr18:29206102..29208678-chr18:29263634..29265873,3	MCF-7	breast:
17	chr18:29259001..29261313-chr18:29272206..29274958,2	MCF-7	breast:
18	chr11:369439..370438-chr18:29265185..29265845,2	MCF-7	breast:
19	chr18:29235239..29238459-chr18:29263541..29266170,4	MCF-7	breast:
20	chr18:29225539..29227273-chr18:29351127..29353466,2	K562	blood:
21	chr18:29257336..29259422-chr18:29266158..29267928,2	K562	blood:
22	chr18:29209445..29212073-chr18:29221671..29224174,2	K562	blood:
23	chr18:29219456..29221928-chr18:29224647..29227313,2	K562	blood:
24	chr18:29235060..29236900-chr18:29250262..29252488,2	MCF-7	breast:
25	chr18:29238110..29240521-chr18:29255688..29258498,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTR-1	chr18:29264688-29267822	NONHSAT058829
2	lnc-TTR-1	chr18:29265618-29266786	ENSG00000259985.1

No data

Variant related genes	Relation type
B4GALT6	TF binding region
RNU6-1002P	TF binding region
ENSG00000259985	TF binding region
B4GALT6	CpG island
RNU6-1002P	CpG island
ENSG00000259985	CpG island
ENSG00000118276	chromatin interactions
ENSG00000259985	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000182272	chromatin interactions

Extended variants
information (count: 2381 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377500778	chr18:29205538-29205539	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs201381453	chr18:29205546-29205547	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200977259	chr18:29205559-29205560	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375568606	chr18:29205562-29205563	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188400501	chr18:29205563-29205564	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs201116758	chr18:29205564-29205565	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34683195	chr18:29205591-29205592	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs372756128	chr18:29205593-29205594	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530982610	chr18:29205595-29205596	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374433903	chr18:29205610-29205611	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113933016	chr18:29205622-29205623	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371220404	chr18:29205624-29205625	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111402923	chr18:29205646-29205647	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76837639	chr18:29205651-29205652	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116094076	chr18:29205664-29205665	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375001901	chr18:29205685-29205686	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139384688	chr18:29205691-29205692	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150100199	chr18:29205726-29205727	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200258231	chr18:29205736-29205737	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74719321	chr18:29205758-29205759	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34625849	chr18:29205769-29205770	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs151309842	chr18:29205772-29205773	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371138643	chr18:29205774-29205775	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140540557	chr18:29205791-29205792	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150496041	chr18:29205817-29205818	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576228273	chr18:29205839-29205840	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183844436	chr18:29205881-29205882	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368060475	chr18:29205931-29205932	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138536097	chr18:29205932-29205933	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141969960	chr18:29205934-29205935	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538251857	chr18:29205951-29205952	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4799588	chr18:29205953-29205954	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576398101	chr18:29205986-29205987	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537470961	chr18:29206013-29206014	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs555768875	chr18:29206014-29206015	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs574180856	chr18:29206025-29206026	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs541949622	chr18:29206026-29206027	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs576489461	chr18:29206030-29206031	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs577028925	chr18:29206033-29206034	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs371815553	chr18:29206057-29206058	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs541916297	chr18:29206058-29206059	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs573387513	chr18:29206076-29206077	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs111489083	chr18:29206106-29206107	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs3764474	chr18:29206121-29206122	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565591304	chr18:29206154-29206155	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs138746723	chr18:29206166-29206167	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs117100417	chr18:29206194-29206195	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572292278	chr18:29206205-29206206	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550970377	chr18:29206217-29206218	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs370138673	chr18:29206228-29206229	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1715 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29191400-29207000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr18:29191400-29207800	Weak transcription	Fetal Intestine Large	intestine
3	chr18:29191800-29207800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr18:29192200-29206200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr18:29192400-29217400	Weak transcription	Left Ventricle	heart
6	chr18:29194800-29226800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr18:29195600-29206000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr18:29197200-29210600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr18:29197400-29207800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr18:29197600-29206400	Weak transcription	Fetal Intestine Small	intestine
11	chr18:29197600-29224800	Weak transcription	Brain Anterior Caudate	brain
12	chr18:29197600-29224800	Weak transcription	Brain Germinal Matrix	brain
13	chr18:29197800-29206200	Weak transcription	GM12878-XiMat	blood
14	chr18:29199200-29212400	Weak transcription	Aorta	Aorta
15	chr18:29199800-29217200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr18:29200000-29222400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr18:29200200-29208600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr18:29200200-29222000	Weak transcription	HMEC	breast
19	chr18:29200400-29210400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr18:29200800-29206600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr18:29201600-29206200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr18:29202800-29235000	Weak transcription	Pancreas	Pancrea
23	chr18:29202800-29240200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr18:29203000-29208000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr18:29203200-29217000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr18:29203400-29211000	Weak transcription	HUVEC	blood vessel
27	chr18:29203800-29207800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr18:29203800-29220200	Weak transcription	Ovary	ovary
29	chr18:29203800-29226000	Weak transcription	Fetal Lung	lung
30	chr18:29203800-29227400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr18:29204000-29210000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr18:29204000-29210400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr18:29204000-29210400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr18:29204000-29213600	Weak transcription	Thymus	Thymus
35	chr18:29204000-29228400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr18:29204200-29223200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr18:29204400-29220800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr18:29204400-29228400	Weak transcription	Psoas Muscle	Psoas
39	chr18:29204600-29205800	Enhancers	HepG2	liver
40	chr18:29204600-29213600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr18:29204600-29238600	Weak transcription	Gastric	stomach
42	chr18:29204800-29206200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr18:29204800-29206200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr18:29204800-29206400	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr18:29204800-29206400	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr18:29204800-29208200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr18:29204800-29209000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr18:29204800-29209000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr18:29205000-29215600	Weak transcription	Fetal Stomach	stomach
50	chr18:29205000-29215800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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