Variant report

Variant	nsv1065285
Chromosome Location	chr18:29527884-29614986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1215)
CpG islands
(count:857)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1215 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29537022-29537114	K562	blood:	n/a	n/a
2	ARID3A	chr18:29534309-29534712	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29545658-29545826	K562	blood:	n/a	n/a
4	ARID3A	chr18:29598287-29598586	K562	blood:	n/a	n/a
5	ARID3A	chr18:29532310-29532545	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29557292-29557535	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:29557377-29557689	K562	blood:	n/a	n/a
8	ATF1	chr18:29598201-29598753	K562	blood:	n/a	n/a
9	ATF2	chr18:29598266-29598843	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr18:29598243-29598823	GM12878	blood:	n/a	n/a
11	ATF2	chr18:29536816-29537133	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr18:29598246-29598774	GM12878	blood:	n/a	n/a
13	ATF2	chr18:29590048-29590496	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr18:29557219-29557644	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr18:29570743-29571182	GM12878	blood:	n/a	n/a
16	BACH1	chr18:29557332-29557688	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr18:29598998-29599076	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr18:29557475-29557490	K562	blood:	n/a	n/a
19	BCL11A	chr18:29570839-29571146	GM12878	blood:	n/a	n/a
20	BCL11A	chr18:29570849-29571082	GM12878	blood:	n/a	n/a
21	BCLAF1	chr18:29598297-29598917	GM12878	blood:	n/a	chr18:29598627-29598640 chr18:29598573-29598586 chr18:29598587-29598596 chr18:29598673-29598682 chr18:29598626-29598639 chr18:29598692-29598705
22	BCLAF1	chr18:29598288-29599107	GM12878	blood:	n/a	chr18:29598627-29598640 chr18:29598573-29598586 chr18:29598587-29598596 chr18:29598673-29598682 chr18:29598626-29598639 chr18:29598692-29598705
23	BCLAF1	chr18:29570709-29571250	GM12878	blood:	n/a	n/a
24	BCLAF1	chr18:29599513-29599997	GM12878	blood:	n/a	n/a
25	BHLHE40	chr18:29534377-29534734	HepG2	liver:	n/a	n/a
26	BHLHE40	chr18:29598385-29598942	GM12878	blood:	n/a	chr18:29598572-29598588
27	BHLHE40	chr18:29599317-29599873	GM12878	blood:	n/a	n/a
28	BHLHE40	chr18:29598328-29598768	K562	blood:	n/a	chr18:29598572-29598588
29	BHLHE40	chr18:29599438-29599561	K562	blood:	n/a	n/a
30	BHLHE40	chr18:29534485-29534681	K562	blood:	n/a	n/a
31	BHLHE40	chr18:29536921-29537061	GM12878	blood:	n/a	n/a
32	BHLHE40	chr18:29536920-29537206	K562	blood:	n/a	n/a
33	BHLHE40	chr18:29599279-29599710	HepG2	liver:	n/a	n/a
34	BHLHE40	chr18:29536923-29537211	HepG2	liver:	n/a	n/a
35	BHLHE40	chr18:29557383-29557574	K562	blood:	n/a	n/a
36	BRCA1	chr18:29598267-29598862	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr18:29553933-29554341	HCT-116	colon:	n/a	n/a
38	CBX3	chr18:29598314-29598876	K562	blood:	n/a	n/a
39	CBX3	chr18:29553882-29554264	K562	blood:	n/a	n/a
40	CBX3	chr18:29558690-29558864	K562	blood:	n/a	n/a
41	CBX3	chr18:29558693-29559032	HCT-116	colon:	n/a	n/a
42	CBX3	chr18:29553910-29554272	K562	blood:	n/a	n/a
43	CBX3	chr18:29553788-29554365	HCT-116	colon:	n/a	n/a
44	CBX3	chr18:29558692-29558957	K562	blood:	n/a	n/a
45	CCNT2	chr18:29598329-29599338	K562	blood:	n/a	n/a
46	CEBPB	chr18:29534364-29534676	A549	lung:	n/a	chr18:29534509-29534520
47	CEBPB	chr18:29612642-29612889	K562	blood:	n/a	chr18:29612772-29612783
48	CEBPB	chr18:29534279-29534721	Hela-S3	cervix:	n/a	chr18:29534509-29534520
49	CEBPB	chr18:29534365-29534797	HCT-116	colon:	n/a	chr18:29534509-29534520
50	CEBPB	chr18:29530612-29530819	HepG2	liver:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29599124-29599174	IMR90	lung:	fetal
2	chr18:29598697-29598747	SK-N-SH	brain:	n/a
3	chr18:29598296-29598346	IMR90	lung:	fetal
4	chr18:29599124-29599174	IMR90	lung:	fetal
5	chr18:29598697-29598747	SK-N-SH	brain:	n/a
6	chr18:29598296-29598346	IMR90	lung:	fetal
7	chr18:29599349-29599399	IMR90	lung:	fetal
8	chr18:29598757-29598807	T-47D	breast:	n/a
9	chr18:29598697-29598747	HPAEpiC	pulmonary alveolar:	n/a
10	chr18:29597493-29597543	AG04449	skin:	fetal
11	chr18:29597478-29597528	HAEpiC	amniotic membrane:	n/a
12	chr18:29598437-29598487	PrEC	prostate:	n/a
13	chr18:29598919-29598969	SAEC	small airway:	n/a
14	chr18:29598433-29598483	HRE	kidney:	n/a
15	chr18:29598433-29598483	HCF	heart:	n/a
16	chr18:29599776-29599826	HNPCEpiC	eye:	n/a
17	chr18:29598757-29598807	HCM	heart:	n/a
18	chr18:29596358-29596408	ovcar-3	ovarian:	n/a
19	chr18:29598433-29598483	NH-A	brain:	n/a
20	chr18:29599124-29599174	U87	brain:	n/a
21	chr18:29596358-29596408	A549	lung:	n/a
22	chr18:29598757-29598807	AG09319	gingival:	n/a
23	chr18:29598757-29598807	HCPEpiC	choroid plexus:	n/a
24	chr18:29598757-29598807	SK-N-SH_RA	brain:	n/a
25	chr18:29598919-29598969	PFSK-1	brain:	n/a
26	chr18:29601617-29601667	PANC-1	pancreas:	n/a
27	chr18:29601617-29601667	GM12878	blood:	n/a
28	chr18:29598433-29598483	NT2-D1	testis:	n/a
29	chr18:29598433-29598483	HL-60	blood:	n/a
30	chr18:29596358-29596408	HPAEpiC	pulmonary alveolar:	n/a
31	chr18:29599124-29599174	HRCEpiC	kidney:	n/a
32	chr18:29598697-29598747	MCF10A-Er-Src	breast:	n/a
33	chr18:29599124-29599174	H1-hESC	embryonic stem cell:	embryo
34	chr18:29598757-29598807	IMR90	lung:	fetal
35	chr18:29597493-29597543	Hela-S3	cervix:	n/a
36	chr18:29601617-29601667	HCF	heart:	n/a
37	chr18:29598697-29598747	BJ	skin:	n/a
38	chr18:29597478-29597528	CMK	blood:	n/a
39	chr18:29599776-29599826	Hela-S3	cervix:	n/a
40	chr18:29601617-29601667	HEK293	kidney:	embryo
41	chr18:29599349-29599399	ProgFib	skin:	n/a
42	chr18:29598433-29598483	HEEpiC	esophagus:	n/a
43	chr18:29599776-29599826	Jurkat	blood:	n/a
44	chr18:29599349-29599399	HEK293	kidney:	embryo
45	chr18:29598437-29598487	BJ	skin:	n/a
46	chr18:29598433-29598483	GM19239	blood:	n/a
47	chr18:29598433-29598483	ovcar-3	ovarian:	n/a
48	chr18:29596358-29596408	GM12878	blood:	n/a
49	chr18:29598400-29598450	HCM	heart:	n/a
50	chr18:29599349-29599399	SK-N-MC	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29522234..29525588-chr18:29534457..29537204,4	MCF-7	breast:
2	chr18:29597754..29600118-chr18:29600354..29602293,2	MCF-7	breast:
3	chr18:29522626..29525135-chr18:29528415..29529942,2	K562	blood:
4	chr18:29523716..29526205-chr18:29536614..29539662,3	K562	blood:
5	chr18:29588031..29590764-chr18:29592870..29595455,2	K562	blood:
6	chr18:29598516..29599058-chr2:47168202..47168759,2	Hela-S3	cervix:
7	chr18:29522696..29523369-chr18:29598378..29599258,2	Hela-S3	cervix:
8	chr18:29522249..29524505-chr18:29596603..29599089,2	MCF-7	breast:
9	chr18:29531400..29532947-chr18:29534853..29537297,2	K562	blood:
10	chr18:29599759..29602632-chr18:29612702..29615585,2	K562	blood:
11	chr18:29521665..29524441-chr18:29544834..29547590,2	K562	blood:
12	chr18:29522629..29525199-chr18:29571668..29573171,2	K562	blood:
13	chr18:29596689..29599956-chr18:29670764..29674475,6	MCF-7	breast:
14	chr18:29598566..29600531-chr18:29604153..29606634,2	MCF-7	breast:
15	chr18:29597700..29599894-chr18:29602384..29604924,2	K562	blood:
16	chr18:29570336..29572597-chr18:29669436..29671957,2	K562	blood:
17	chr18:29598540..29599388-chr18:29671670..29672456,2	Hela-S3	cervix:
18	chr18:29598053..29598969-chr6:27114842..27115533,2	Hela-S3	cervix:
19	chr18:29597506..29599866-chr18:29670953..29673378,4	MCF-7	breast:
20	chr18:29588031..29590764-chr18:29592870..29595455,2	K562	blood:
21	chr18:29531400..29532947-chr18:29534853..29537297,2	K562	blood:
22	chr18:29599759..29602632-chr18:29612702..29615585,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRAPPC8-3	chr18:29533013-29533099	NONHSAT058843

No data

Variant related genes	Relation type
PGDP1	TF binding region
TRAPPC8	TF binding region
ENSG00000263917	TF binding region
RNF125	TF binding region
ENSG00000266105	TF binding region
PGDP1	CpG island
TRAPPC8	CpG island
ENSG00000263917	CpG island
RNF125	CpG island
ENSG00000266105	CpG island
ENSG00000153339	chromatin interactions
ENSG00000068724	chromatin interactions
ENSG00000101695	chromatin interactions
ENSG00000134758	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000238982	chromatin interactions
ENSG00000265008	chromatin interactions
ENSG00000263917	chromatin interactions
ENSG00000263823	chromatin interactions
ENSG00000184825	chromatin interactions

Extended variants
information (count: 3340 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3340 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11661310	chr18:29527884-29527885	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189925533	chr18:29527956-29527957	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533475625	chr18:29528058-29528059	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370869956	chr18:29528076-29528077	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545279305	chr18:29528077-29528078	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116235577	chr18:29528102-29528103	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544978205	chr18:29528109-29528110	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530903945	chr18:29528126-29528127	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563372518	chr18:29528150-29528151	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530591119	chr18:29528162-29528163	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567710915	chr18:29528163-29528164	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542470530	chr18:29528187-29528188	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34329580	chr18:29528226-29528227	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs7244322	chr18:29528233-29528234	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs182008506	chr18:29528236-29528237	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565776657	chr18:29528268-29528269	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557265453	chr18:29528347-29528348	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138353273	chr18:29528380-29528381	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536206740	chr18:29528425-29528426	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551334322	chr18:29528426-29528427	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554261194	chr18:29528471-29528472	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs144055072	chr18:29528477-29528478	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186240820	chr18:29528484-29528485	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147144292	chr18:29528498-29528499	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35796812	chr18:29528535-29528536	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553184287	chr18:29528545-29528546	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537539045	chr18:29528547-29528548	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140266727	chr18:29528559-29528560	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549341365	chr18:29528602-29528603	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142684974	chr18:29528629-29528630	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190705150	chr18:29528646-29528647	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543048730	chr18:29528659-29528660	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147387067	chr18:29528668-29528669	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535050580	chr18:29528731-29528732	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528623276	chr18:29528733-29528734	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553715395	chr18:29528757-29528758	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs111966565	chr18:29528780-29528781	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532298654	chr18:29528830-29528831	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148425987	chr18:29528854-29528855	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs538657399	chr18:29528861-29528862	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201315319	chr18:29528865-29528866	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs199507196	chr18:29528881-29528882	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569176259	chr18:29528907-29528908	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs536155475	chr18:29528917-29528918	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548198264	chr18:29528965-29528966	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566116582	chr18:29528972-29528973	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs180869102	chr18:29528988-29528989	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs185808077	chr18:29529029-29529030	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577817563	chr18:29529033-29529034	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191498829	chr18:29529056-29529057	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29524600-29530600	Weak transcription	Brain Angular Gyrus	brain
2	chr18:29524800-29530800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr18:29525000-29530400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr18:29525000-29530400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr18:29525400-29528400	Weak transcription	K562	blood
6	chr18:29525600-29537400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr18:29525800-29530000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr18:29526800-29529400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr18:29527200-29530000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr18:29527400-29530000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr18:29527600-29528800	Enhancers	Fetal Intestine Large	intestine
12	chr18:29527600-29528800	Enhancers	Fetal Intestine Small	intestine
13	chr18:29527800-29528200	Enhancers	HepG2	liver
14	chr18:29527800-29528400	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr18:29528200-29530200	Weak transcription	HepG2	liver
16	chr18:29528400-29528800	Enhancers	K562	blood
17	chr18:29528800-29530400	Weak transcription	Fetal Intestine Small	intestine
18	chr18:29528800-29530600	Weak transcription	Fetal Intestine Large	intestine
19	chr18:29528800-29533400	Weak transcription	K562	blood
20	chr18:29529200-29529800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr18:29530000-29530800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr18:29530000-29530800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr18:29530000-29530800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr18:29530000-29530800	Enhancers	Brain Germinal Matrix	brain
25	chr18:29530000-29531000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr18:29530000-29531400	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr18:29530000-29532400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr18:29530000-29532600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr18:29530200-29531000	Enhancers	HepG2	liver
30	chr18:29530200-29531200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr18:29530400-29530800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr18:29530400-29530800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr18:29530400-29530800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr18:29530400-29531000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr18:29530400-29531200	Enhancers	Fetal Intestine Small	intestine
36	chr18:29530400-29532000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr18:29530600-29530800	Enhancers	Brain Angular Gyrus	brain
38	chr18:29530600-29531000	Enhancers	Fetal Intestine Large	intestine
39	chr18:29530600-29531200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr18:29530800-29531400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr18:29530800-29534400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr18:29530800-29534600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr18:29531000-29531200	Enhancers	Small Intestine	intestine
44	chr18:29531000-29532000	Weak transcription	HepG2	liver
45	chr18:29531000-29533800	Weak transcription	Fetal Intestine Large	intestine
46	chr18:29531000-29534400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr18:29531200-29533400	Weak transcription	Small Intestine	intestine
48	chr18:29531200-29533600	Weak transcription	Fetal Intestine Small	intestine
49	chr18:29531200-29534200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr18:29531400-29534200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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