Variant report

Variant	nsv528699
Chromosome Location	chr18:11989416-12029857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:866)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:12008355-12008698	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:11994407-11994903	HepG2	liver:	n/a	n/a
3	BACH1	chr18:11994815-11995014	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr18:12005731-12006073	GM12878	blood:	n/a	chr18:12005927-12005937 chr18:12005953-12005963 chr18:12005926-12005937
5	BCL3	chr18:12023118-12023602	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:11995405-11995960	K562	blood:	n/a	n/a
7	BHLHE40	chr18:12008250-12009049	HepG2	liver:	n/a	chr18:12008904-12008920
8	BHLHE40	chr18:11994362-11995230	HepG2	liver:	n/a	n/a
9	BHLHE40	chr18:11995507-11995749	GM12878	blood:	n/a	n/a
10	BRCA1	chr18:11994404-11994734	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr18:11995458-11995739	K562	blood:	n/a	n/a
12	CEBPB	chr18:12013302-12013366	HepG2	liver:	n/a	n/a
13	CEBPB	chr18:11994360-11994783	A549	lung:	n/a	chr18:11994620-11994633
14	CEBPB	chr18:12027473-12027797	IMR90	lung:	n/a	chr18:12027630-12027641
15	CEBPB	chr18:12027491-12027786	ECC-1	luminal epithelium:	n/a	chr18:12027630-12027641
16	CEBPB	chr18:11995363-11995735	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr18:11994273-11994916	Hela-S3	cervix:	n/a	chr18:11994620-11994633
18	CEBPB	chr18:12027616-12027655	Hela-S3	cervix:	n/a	chr18:12027630-12027641
19	CEBPB	chr18:12008328-12008616	HepG2	liver:	n/a	n/a
20	CEBPB	chr18:12015411-12015989	IMR90	lung:	n/a	chr18:12015549-12015560 chr18:12015549-12015562
21	CEBPB	chr18:12027564-12027728	HepG2	liver:	n/a	chr18:12027630-12027641
22	CEBPB	chr18:12027530-12027785	A549	lung:	n/a	chr18:12027630-12027641
23	CEBPB	chr18:12015564-12016042	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr18:12011847-12012042	IMR90	lung:	n/a	n/a
25	CEBPB	chr18:12027470-12027810	HepG2	liver:	n/a	chr18:12027630-12027641
26	CEBPB	chr18:11994290-11994925	HepG2	liver:	n/a	chr18:11994620-11994633
27	CEBPB	chr18:12027461-12027806	H1-hESC	embryonic stem cell:	n/a	chr18:12027630-12027641
28	CEBPB	chr18:12027466-12027820	HepG2	liver:	n/a	chr18:12027630-12027641
29	CEBPB	chr18:12027584-12027784	K562	blood:	n/a	chr18:12027630-12027641
30	CEBPB	chr18:12015609-12015983	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr18:11994402-11994598	HepG2	liver:	n/a	n/a
32	CEBPB	chr18:11994308-11994898	HepG2	liver:	n/a	chr18:11994620-11994633
33	CEBPB	chr18:12021199-12021495	HepG2	liver:	n/a	chr18:12021338-12021349
34	CEBPB	chr18:11998768-11998855	K562	blood:	n/a	n/a
35	CEBPB	chr18:11998838-11999031	HepG2	liver:	n/a	chr18:11998877-11998888
36	CEBPB	chr18:11994315-11994893	IMR90	lung:	n/a	chr18:11994620-11994633
37	CEBPB	chr18:12021220-12021383	HepG2	liver:	n/a	chr18:12021338-12021349
38	CEBPB	chr18:12021203-12021517	HepG2	liver:	n/a	chr18:12021338-12021349
39	CEBPB	chr18:12013318-12013444	K562	blood:	n/a	n/a
40	CEBPB	chr18:11994284-11994648	MCF-7	breast:	n/a	chr18:11994620-11994633
41	CEBPB	chr18:11994309-11994708	HepG2	liver:	n/a	chr18:11994620-11994633
42	CEBPB	chr18:12015497-12016059	ECC-1	luminal epithelium:	n/a	chr18:12015549-12015560 chr18:12015549-12015562
43	CEBPB	chr18:11994228-11994770	A549	lung:	n/a	chr18:11994620-11994633
44	CEBPD	chr18:12008382-12008611	HepG2	liver:	n/a	n/a
45	CEBPD	chr18:11994449-11994605	HepG2	liver:	n/a	n/a
46	CHD1	chr18:11995146-11995871	IMR90	lung:	n/a	n/a
47	CHD2	chr18:11994866-11995711	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr18:12015374-12015377	HepG2	liver:	n/a	n/a
49	CHD2	chr18:11994328-11995023	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr18:11995405-11995638	HepG2	liver:	n/a	n/a

No data

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12015892..12018624-chr18:12025559..12027409,2	K562	blood:
2	chr18:11980570..11987752-chr18:11988318..11993643,9	K562	blood:
3	chr18:11993860..11995510-chr18:12012854..12014653,2	K562	blood:
4	chr18:11937961..11938594-chr18:11989491..11990037,2	MCF-7	breast:
5	chr18:11908518..11911302-chr18:12009524..12011140,2	MCF-7	breast:
6	chr18:11980368..11983094-chr18:12003809..12006804,4	MCF-7	breast:
7	chr18:11997422..12000710-chr18:12005717..12008163,3	K562	blood:
8	chr18:11913714..11914470-chr18:11995363..11996159,2	MCF-7	breast:
9	chr18:11980799..11981701-chr18:11992889..11993744,2	Hela-S3	cervix:
10	chr18:11978568..11983192-chr18:11993805..11998306,5	MCF-7	breast:
11	chr18:12025555..12027976-chr18:12028619..12030454,2	K562	blood:
12	chr18:11980409..11982733-chr18:12000463..12003199,2	MCF-7	breast:
13	chr18:12017282..12018907-chr18:12020565..12022522,2	K562	blood:
14	chr18:12017282..12018907-chr18:12020565..12022522,2	K562	blood:
15	chr18:12006542..12008097-chr18:12010125..12012103,2	MCF-7	breast:
16	chr18:12006542..12008097-chr18:12010125..12012103,2	MCF-7	breast:
17	chr18:12009084..12011598-chr18:12022271..12024382,2	MCF-7	breast:
18	chr18:12006195..12007713-chr18:12008084..12010111,2	MCF-7	breast:
19	chr18:12000492..12002135-chr18:12004782..12007391,2	MCF-7	breast:
20	chr18:11905031..11907114-chr18:12010048..12012085,2	K562	blood:
21	chr18:11949879..11951567-chr18:11988401..11991255,2	K562	blood:
22	chr18:11978843..11982198-chr18:12003396..12007810,5	MCF-7	breast:
23	chr18:11993441..11996170-chr18:12004399..12006022,2	MCF-7	breast:
24	chr18:12000492..12002135-chr18:12004782..12007391,2	MCF-7	breast:
25	chr18:12005936..12008667-chr18:12037616..12040479,2	MCF-7	breast:
26	chr18:11849319..11851808-chr18:12002886..12005709,2	MCF-7	breast:
27	chr18:11654974..11655700-chr18:11995123..11996004,2	K562	blood:
28	chr18:11992964..11995381-chr18:12038056..12040567,2	MCF-7	breast:
29	chr18:11937478..11938603-chr18:11995051..11996237,21	K562	blood:
30	chr18:11906470..11908807-chr18:12016802..12018386,2	MCF-7	breast:
31	chr18:11978630..11983643-chr18:11987662..11991726,6	MCF-7	breast:
32	chr18:12025555..12027976-chr18:12028619..12030454,2	K562	blood:
33	chr18:12015892..12018624-chr18:12025559..12027409,2	K562	blood:
34	chr18:11994002..11996965-chr18:12008009..12011015,3	MCF-7	breast:
35	chr18:11979171..11983679-chr18:11993501..11995734,4	MCF-7	breast:
36	chr18:11987852..11990240-chr18:11991809..11994085,2	K562	blood:
37	chr18:11937069..11938706-chr18:11995081..11996087,16	MCF-7	breast:
38	chr18:11990931..11993747-chr18:11994140..11995765,2	K562	blood:
39	chr18:11994002..11996965-chr18:12008009..12011015,3	MCF-7	breast:
40	chr18:11987852..11990240-chr18:11991809..11994085,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP002414.1.1-4	chr18:11994795-11994937	ENSG00000266955.1
2	lnc-AP002414.1.1-4	chr18:11993987-11994371	ENSG00000266955.1

No data

Variant related genes	Relation type
ENSG00000266955	TF binding region
IMPA2	TF binding region
ENSG00000267079	chromatin interactions
ENSG00000141401	chromatin interactions
ENSG00000255112	chromatin interactions
ENSG00000154889	chromatin interactions
ENSG00000266995	chromatin interactions
ENSG00000266955	chromatin interactions
ENSG00000273141	chromatin interactions

Extended variants
information (count: 1770 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs663591	chr18:11989416-11989417	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs386801328	chr18:11989435-11989436	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs653073	chr18:11989436-11989437	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs565416216	chr18:11989450-11989451	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs369062864	chr18:11989477-11989478	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs577162627	chr18:11989507-11989508	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187038395	chr18:11989529-11989530	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs113918556	chr18:11989531-11989532	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190322298	chr18:11989537-11989538	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182769741	chr18:11989539-11989540	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs652602	chr18:11989557-11989558	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs79027352	chr18:11989592-11989593	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551839761	chr18:11989612-11989613	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570494055	chr18:11989632-11989633	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534606189	chr18:11989648-11989649	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546280710	chr18:11989692-11989693	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150262952	chr18:11989717-11989718	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535771890	chr18:11989725-11989726	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557322552	chr18:11989739-11989740	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575498251	chr18:11989781-11989782	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113531299	chr18:11989792-11989793	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559007239	chr18:11989812-11989813	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs577269949	chr18:11989818-11989819	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs7231196	chr18:11989823-11989824	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559504927	chr18:11989844-11989845	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565065489	chr18:11989922-11989923	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532563185	chr18:11989934-11989935	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs576171843	chr18:11989941-11989942	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs650727	chr18:11989969-11989970	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs542094494	chr18:11989999-11990000	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187456203	chr18:11990000-11990001	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192978108	chr18:11990023-11990024	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531000298	chr18:11990074-11990075	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145820118	chr18:11990112-11990113	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370163830	chr18:11990155-11990156	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs649713	chr18:11990200-11990201	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs538865919	chr18:11990205-11990206	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs649396	chr18:11990227-11990228	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs148970167	chr18:11990291-11990292	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143080261	chr18:11990309-11990310	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185684957	chr18:11990324-11990325	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs655409	chr18:11990346-11990347	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs200120691	chr18:11990355-11990356	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs58393627	chr18:11990357-11990358	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374600002	chr18:11990358-11990359	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373865206	chr18:11990359-11990360	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557678248	chr18:11990376-11990377	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs655790	chr18:11990381-11990382	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534830405	chr18:11990428-11990429	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs638125	chr18:11990470-11990471	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

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
Autism	20808228	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
small cell lung cancer	20016488	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	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
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1670 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11982400-12005000	Weak transcription	Aorta	Aorta
2	chr18:11982600-11995600	Weak transcription	Primary T cells from cord blood	blood
3	chr18:11982600-11995800	Weak transcription	Thymus	Thymus
4	chr18:11982600-12028600	Weak transcription	Small Intestine	intestine
5	chr18:11983400-11989600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr18:11983400-11994000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr18:11984200-11989800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr18:11984200-11993600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr18:11984200-11994600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr18:11984400-11989600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr18:11984400-11990000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr18:11984400-11990400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr18:11984400-11993400	Weak transcription	Lung	lung
14	chr18:11984400-11994200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr18:11984400-11994200	Weak transcription	NHEK	skin
16	chr18:11984400-11995000	Weak transcription	GM12878-XiMat	blood
17	chr18:11984600-11989800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr18:11985200-11991200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr18:11986000-11990400	Weak transcription	Fetal Kidney	kidney
20	chr18:11986000-11995600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr18:11986400-11990000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr18:11986400-11994600	Weak transcription	Liver	Liver
23	chr18:11986600-11990800	Weak transcription	Ovary	ovary
24	chr18:11986800-11990200	Enhancers	A549	lung
25	chr18:11986800-11992800	Enhancers	Fetal Muscle Trunk	muscle
26	chr18:11987200-11989600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr18:11987200-11990400	Genic enhancers	Hela-S3	cervix
28	chr18:11987200-11994800	Weak transcription	Right Atrium	heart
29	chr18:11987400-11991200	Enhancers	Fetal Lung	lung
30	chr18:11987600-11992400	Enhancers	Fetal Muscle Leg	muscle
31	chr18:11987800-11991400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr18:11988000-11991800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr18:11988000-11995600	Weak transcription	K562	blood
34	chr18:11988200-11990200	Enhancers	Duodenum Mucosa	Duodenum
35	chr18:11988200-11991600	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr18:11988400-11989600	Enhancers	HSMMtube	muscle
37	chr18:11988400-11989800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr18:11988400-11990600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr18:11988400-11990800	Enhancers	Stomach Mucosa	stomach
40	chr18:11988400-11991600	Enhancers	Esophagus	oesophagus
41	chr18:11988400-11991600	Enhancers	Psoas Muscle	Psoas
42	chr18:11988600-11989800	Enhancers	Left Ventricle	heart
43	chr18:11988600-11990600	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr18:11988600-11991800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr18:11988600-11995200	Weak transcription	Primary hematopoietic stem cells	blood
46	chr18:11988800-11990000	Enhancers	Colonic Mucosa	Colon
47	chr18:11988800-11990400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr18:11988800-11990400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr18:11988800-11990400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr18:11988800-11990800	Enhancers	HUES48 Cell Line	embryonic stem cell

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