Variant report

Variant	nsv576542
Chromosome Location	chr18:14913292-14978677
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	chr18:14919804-14920000	HepG2	liver:	n/a	n/a
2	ATF1	chr18:14971054-14971139	K562	blood:	n/a	n/a
3	BHLHE40	chr18:14919900-14920096	K562	blood:	n/a	n/a
4	CEBPB	chr18:14974278-14974509	HepG2	liver:	n/a	chr18:14974416-14974427 chr18:14974350-14974361
5	CEBPB	chr18:14946395-14946563	HepG2	liver:	n/a	chr18:14946440-14946451
6	CTCF	chr18:14963426-14963535	MCF-7	breast:	n/a	n/a
7	CTCF	chr18:14922286-14922288	LNCaP	prostate:	n/a	n/a
8	CTCF	chr18:14976870-14976976	Fibrobl	skin:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
9	CTCF	chr18:14944263-14944463	MCF-7	breast:	n/a	chr18:14944372-14944390 chr18:14944375-14944384
10	CTCF	chr18:14941393-14941483	Pancreas_OC	pancreas:	n/a	n/a
11	CTCF	chr18:14944302-14944575	MCF-7	breast:	n/a	chr18:14944372-14944390 chr18:14944375-14944384
12	CTCF	chr18:14976897-14976964	GM12891	blood:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
13	CTCF	chr18:14976836-14977036	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
14	CTCF	chr18:14976880-14977030	HMEC	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
15	CTCF	chr18:14936820-14936970	GM12868	blood:	n/a	n/a
16	CTCF	chr18:14921769-14921819	LNCaP	prostate:	n/a	n/a
17	CTCF	chr18:14976820-14976970	AG04449	skin:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
18	CTCF	chr18:14976893-14976967	Hela-S3	cervix:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
19	CTCF	chr18:14922240-14922390	MCF-7	breast:	n/a	n/a
20	CTCF	chr18:14935462-14935551	MCF-7	breast:	n/a	chr18:14935497-14935515 chr18:14935504-14935512
21	CTCF	chr18:14944300-14944450	HEK293	kidney:	n/a	chr18:14944372-14944390 chr18:14944375-14944384
22	CTCF	chr18:14976800-14976950	HMEC	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
23	CTCF	chr18:14922203-14922244	LNCaP	prostate:	n/a	n/a
24	CTCF	chr18:14944273-14944464	MCF-7	breast:	n/a	chr18:14944372-14944390 chr18:14944375-14944384
25	CTCF	chr18:14915040-14915165	ProgFib	skin:	n/a	n/a
26	CTCF	chr18:14976820-14976970	HRE	kidney:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
27	CTCF	chr18:14943707-14943739	Fibrobl	skin:	n/a	n/a
28	CTCF	chr18:14976820-14976970	HCFaa	heart:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
29	CTCF	chr18:14922121-14922338	MCF-7	breast:	n/a	n/a
30	CTCF	chr18:14976848-14977015	K562	blood:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
31	CTCF	chr18:14944270-14944480	MCF-7	breast:	n/a	chr18:14944372-14944390 chr18:14944375-14944384
32	CTCF	chr18:14976820-14976970	HepG2	liver:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
33	CTCF	chr18:14976885-14976942	Pancreas_OC	pancreas:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
34	CTCF	chr18:14976839-14976972	SK-N-SH_RA	brain:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
35	CTCF	chr18:14922122-14922412	MCF-7	breast:	n/a	n/a
36	CTCF	chr18:14976840-14976990	HEK293	kidney:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
37	CTCF	chr18:14915120-14915270	AG10803	skin:	n/a	n/a
38	CTCF	chr18:14944300-14944450	SK-N-SH_RA	brain:	n/a	chr18:14944372-14944390 chr18:14944375-14944384
39	CTCF	chr18:14965760-14965910	GM12871	blood:	n/a	n/a
40	CTCF	chr18:14976843-14977018	HUVEC	blood vessel:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
41	CTCF	chr18:14976860-14977010	NB4	blood:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
42	CTCF	chr18:14976840-14976990	MCF-7	breast:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
43	CTCF	chr18:14976840-14976990	HBMEC	blood vessel:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
44	CTCF	chr18:14923776-14923828	GM20000	blood:	n/a	n/a
45	CTCF	chr18:14976831-14977042	Gliobla	brain:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
46	CTCF	chr18:14976840-14976990	SK-N-SH_RA	brain:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
47	CTCF	chr18:14921929-14922390	MCF-7	breast:	n/a	n/a
48	CTCF	chr18:14976820-14976970	HA-sp	spinal cord:	n/a	chr18:14976928-14976937 chr18:14976922-14976940 chr18:14976925-14976935 chr18:14976921-14976934 chr18:14976924-14976937 chr18:14976899-14976908 chr18:14976917-14976938
49	CTCF	chr18:14944340-14944490	MCF-7	breast:	n/a	chr18:14944372-14944390 chr18:14944375-14944384
50	CTCF	chr18:14922129-14922329	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:14921268..14923858-chr18:14933447..14934992,2	K562	blood:
2	chr18:14921268..14923858-chr18:14933447..14934992,2	K562	blood:
3	chr18:14955184..14958029-chr18:14978854..14981375,2	MCF-7	breast:
4	chr18:14952155..14952955-chr7:115149293..115150054,2	MCF-7	breast:
5	chr18:14919425..14921650-chr18:14925598..14927538,2	MCF-7	breast:
6	chr18:14944732..14947248-chr18:14957647..14959908,2	MCF-7	breast:
7	chr18:14940976..14942480-chr18:14946479..14948653,2	MCF-7	breast:
8	chr18:14940976..14942480-chr18:14946479..14948653,2	MCF-7	breast:
9	chr18:14970038..14971592-chr18:14972164..14974948,2	MCF-7	breast:
10	chr18:14919425..14921650-chr18:14925598..14927538,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD30B-4	chr18:14962069-14962282	ENSG00000266554.1
2	lnc-ANKRD30B-4	chr18:14946266-14946327	ENSG00000266554.1
3	lnc-POTEC-3	chr18:14969000-14969571	ENSG00000264301.1
4	lnc-ANKRD30B-2	chr18:14915514-14915627	ENSG00000263618.1
5	lnc-ANKRD30B-4	chr18:14972355-14973738	ENSG00000266554.1
6	lnc-ANKRD30B-4	chr18:14972377-14973769	ENSG00000266554.1
7	lnc-ANKRD30B-3	chr18:14918961-14919040	XLOC_012636
8	lnc-ANKRD30B-4	chr18:14946266-14946327	NR_104164
9	lnc-ANKRD30B-3	chr18:14929910-14929997	XLOC_012636
10	lnc-ANKRD30B-4	chr18:14965616-14965809	ENSG00000266554.1
11	lnc-ANKRD30B-4	chr18:14971496-14971885	ENSG00000266554.1
12	lnc-POTEC-3	chr18:14969605-14969777	ENSG00000264301.1
13	lnc-POTEC-3	chr18:14969877-14970467	ENSG00000264301.1
14	lnc-ANKRD30B-3	chr18:14930444-14931880	XLOC_012636
15	lnc-ANKRD30B-4	chr18:14965616-14965809	NR_104164
16	lnc-ANKRD30B-4	chr18:14972355-14973755	NR_104164
17	lnc-ANKRD30B-4	chr18:14962069-14962282	NR_104164
18	lnc-POTEC-3	chr18:14969675-14969756	ENSG00000264301.1

Variant related genes	Relation type
ENSG00000264301	TF binding region
ENSG00000266554	TF binding region
ENSG00000263821	TF binding region
ENSG00000264301	chromatin interactions
ENSG00000266554	chromatin interactions

Extended variants
information (count: 2519 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2519 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs786006	chr18:14913292-14913293	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs8089845	chr18:14913334-14913335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573569317	chr18:14913385-14913386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183179751	chr18:14913486-14913487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188252090	chr18:14913503-14913504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555901625	chr18:14913545-14913546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570785785	chr18:14913555-14913556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201835637	chr18:14913604-14913605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75299878	chr18:14913748-14913749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538033015	chr18:14913750-14913751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565372842	chr18:14913761-14913762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73431640	chr18:14913765-14913766	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556361920	chr18:14913823-14913824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115796742	chr18:14913854-14913855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561289584	chr18:14913922-14913923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574557583	chr18:14913961-14913962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116298816	chr18:14913962-14913963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs786005	chr18:14913972-14913973	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs192958587	chr18:14913973-14913974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113041108	chr18:14913994-14913995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535898496	chr18:14914017-14914018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1518583	chr18:14914053-14914054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552529226	chr18:14914157-14914158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75685869	chr18:14914206-14914207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533671293	chr18:14914212-14914213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73431642	chr18:14914222-14914223	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs185219316	chr18:14914263-14914264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113282193	chr18:14914264-14914265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572077540	chr18:14914334-14914335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs786004	chr18:14914367-14914368	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs114793680	chr18:14914381-14914382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544400291	chr18:14914391-14914392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188800410	chr18:14914434-14914435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558499751	chr18:14914449-14914450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572475862	chr18:14914558-14914559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1818658	chr18:14914561-14914562	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs115593956	chr18:14914576-14914577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574881727	chr18:14914593-14914594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192586687	chr18:14914613-14914614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564418693	chr18:14914642-14914643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs786003	chr18:14914643-14914644	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532720022	chr18:14914666-14914667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552707693	chr18:14914673-14914674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559711377	chr18:14914678-14914679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564976326	chr18:14914700-14914701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527338018	chr18:14914705-14914706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547095874	chr18:14914717-14914718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144246303	chr18:14914786-14914787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78521355	chr18:14914792-14914793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs786002	chr18:14914854-14914855	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	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
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14912600-14915200	Enhancers	Osteobl	bone
2	chr18:14914000-14914200	Enhancers	NHDF-Ad	bronchial
3	chr18:14914200-14914800	Weak transcription	NHDF-Ad	bronchial
4	chr18:14914200-14915200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr18:14914400-14914600	Enhancers	Placenta	Placenta
6	chr18:14914400-14915000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr18:14914600-14915200	Weak transcription	Placenta	Placenta
8	chr18:14914800-14915200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr18:14914800-14915600	Enhancers	NHDF-Ad	bronchial
10	chr18:14915200-14916200	Enhancers	Placenta	Placenta
11	chr18:14916400-14925200	Weak transcription	Spleen	Spleen
12	chr18:14917000-14917800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr18:14917800-14918800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr18:14918200-14928400	Weak transcription	Aorta	Aorta
15	chr18:14918800-14920600	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr18:14918800-14921000	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr18:14919000-14920200	ZNF genes & repeats	Fetal Intestine Small	intestine
18	chr18:14919000-14920600	Enhancers	HepG2	liver
19	chr18:14919000-14921000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr18:14919200-14919600	Enhancers	Colonic Mucosa	Colon
21	chr18:14919400-14922200	Enhancers	Liver	Liver
22	chr18:14919600-14921200	Weak transcription	Colonic Mucosa	Colon
23	chr18:14919800-14920200	Enhancers	Pancreas	Pancrea
24	chr18:14920000-14920200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr18:14920000-14920200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr18:14920000-14920200	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr18:14920000-14922200	Enhancers	Duodenum Mucosa	Duodenum
28	chr18:14920200-14920600	Enhancers	Fetal Intestine Small	intestine
29	chr18:14920200-14921200	Weak transcription	Pancreas	Pancrea
30	chr18:14920200-14933200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr18:14920400-14921000	Enhancers	Fetal Intestine Large	intestine
32	chr18:14920600-14920800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
33	chr18:14920800-14921200	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr18:14921000-14921400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
35	chr18:14921000-14921600	Weak transcription	Fetal Intestine Large	intestine
36	chr18:14921200-14921400	Enhancers	Pancreas	Pancrea
37	chr18:14921200-14921600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
38	chr18:14921200-14922000	Enhancers	Colonic Mucosa	Colon
39	chr18:14921200-14923200	Enhancers	Placenta	Placenta
40	chr18:14921400-14921600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr18:14921400-14921600	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr18:14921600-14921800	Enhancers	Fetal Intestine Large	intestine
43	chr18:14921600-14922000	Enhancers	Fetal Intestine Small	intestine
44	chr18:14921600-14922000	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr18:14921600-14923000	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr18:14922000-14922200	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr18:14922000-14924600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr18:14922200-14925200	Weak transcription	Liver	Liver
49	chr18:14922200-14925200	Weak transcription	Duodenum Mucosa	Duodenum
50	chr18:14922200-14933000	Weak transcription	Rectal Mucosa Donor 29	rectum

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