Variant report

Variant	nsv576484
Chromosome Location	chr18:11502864-11510900
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	BRCA1	chr18:11506874-11507253	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr18:11509719-11509820	GM10248	blood:	n/a	n/a
3	FOS	chr18:11506906-11507237	HUVEC	blood vessel:	n/a	chr18:11507073-11507081 chr18:11507071-11507083 chr18:11507071-11507082
4	GATA3	chr18:11506904-11507304	SK-N-SH	brain:	n/a	chr18:11507071-11507080
5	MAFK	chr18:11505582-11505638	HepG2	liver:	n/a	chr18:11505609-11505624 chr18:11505610-11505621 chr18:11505609-11505620 chr18:11505609-11505620 chr18:11505609-11505625 chr18:11505608-11505622
6	MAX	chr18:11505132-11505167	HepG2	liver:	n/a	n/a
7	MYC	chr18:11505141-11505192	MCF-7	breast:	n/a	n/a
8	POLR2A	chr18:11505200-11505387	Gliobla	brain:	n/a	n/a
9	RCOR1	chr18:11505152-11505153	K562	blood:	n/a	n/a
10	REST	chr18:11504927-11505428	MCF-7	breast:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
11	REST	chr18:11505049-11505194	GM12878	blood:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
12	REST	chr18:11504923-11505339	PFSK-1	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
13	REST	chr18:11505027-11505269	U87	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
14	REST	chr18:11505061-11505240	PFSK-1	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
15	REST	chr18:11504918-11505442	ECC-1	luminal epithelium:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
16	REST	chr18:11505070-11505256	K562	blood:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
17	REST	chr18:11505011-11505262	HepG2	liver:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
18	REST	chr18:11504840-11505354	GM12878	blood:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
19	REST	chr18:11504987-11505278	K562	blood:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
20	REST	chr18:11504895-11505353	HCT-116	colon:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
21	REST	chr18:11504996-11505290	GM12878	blood:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
22	REST	chr18:11504990-11505260	HepG2	liver:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
23	REST	chr18:11504846-11505363	MCF-7	breast:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
24	REST	chr18:11505076-11505208	PFSK-1	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
25	REST	chr18:11505043-11505253	U87	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
26	REST	chr18:11504911-11505377	U87	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
27	REST	chr18:11504969-11505276	PANC-1	pancreas:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
28	REST	chr18:11504872-11505377	A549	lung:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
29	REST	chr18:11504950-11505367	PANC-1	pancreas:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
30	REST	chr18:11504989-11505331	A549	lung:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
31	REST	chr18:11504919-11505370	HL-60	blood:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
32	REST	chr18:11505014-11505246	PANC-1	pancreas:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
33	REST	chr18:11504943-11505280	H1-hESC	embryonic stem cell:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
34	REST	chr18:11504976-11505340	HepG2	liver:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
35	REST	chr18:11504965-11505295	Hela-S3	cervix:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
36	REST	chr18:11505058-11505234	PANC-1	pancreas:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
37	REST	chr18:11505018-11505372	H1-hESC	embryonic stem cell:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
38	REST	chr18:11505018-11505337	SK-N-SH	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
39	REST	chr18:11504878-11505435	HL-60	blood:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
40	REST	chr18:11505000-11505281	Hela-S3	cervix:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
41	REST	chr18:11505012-11505239	GM12878	blood:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
42	REST	chr18:11504923-11505353	PANC-1	pancreas:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
43	REST	chr18:11504942-11505378	HCT-116	colon:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
44	REST	chr18:11505090-11505235	SK-N-SH	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11505152-11505172 chr18:11505156-11505169
45	REST	chr18:11504822-11505406	PFSK-1	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
46	REST	chr18:11504898-11505458	ECC-1	luminal epithelium:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
47	REST	chr18:11504971-11505359	SK-N-SH	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
48	REST	chr18:11504968-11505306	HepG2	liver:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
49	REST	chr18:11504911-11505345	U87	brain:	n/a	chr18:11505158-11505167 chr18:11505152-11505172 chr18:11504975-11504995 chr18:11505152-11505172 chr18:11504986-11504995 chr18:11505156-11505169
50	TEAD4	chr18:11504911-11505311	A549	lung:	n/a	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC35G4-1	chr18:11505503-11506635	XLOC_012626
2	lnc-SLC35G4-1	chr18:11506756-11506975	ENSG00000267252.1
3	lnc-SLC35G4-1	chr18:11506756-11506982	XLOC_012626
4	lnc-SLC35G4-1	chr18:11506755-11506982	NONHSAT057314
5	lnc-SLC35G4-1	chr18:11504827-11505058	ENSG00000267252.1
6	lnc-SLC35G4-1	chr18:11506756-11506982	ENSG00000267252.1
7	lnc-SLC35G4-1	chr18:11506756-11506967	ENSG00000267252.1
8	lnc-SLC35G4-1	chr18:11506756-11506979	XLOC_012626
9	lnc-SLC35G4-1	chr18:11504827-11505056	XLOC_012626
10	lnc-SLC35G4-1	chr18:11503733-11503883	ENSG00000267252.1
11	lnc-SLC35G4-1	chr18:11506756-11506946	NONHSAT057308
12	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
13	lnc-SLC35G4-1	chr18:11506756-11506982	XLOC_012626
14	lnc-SLC35G4-1	chr18:11503733-11503883	ENSG00000267252.1
15	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
16	lnc-SLC35G4-1	chr18:11506756-11506979	XLOC_012626
17	lnc-SLC35G4-1	chr18:11505778-11505923	ENSG00000267252.1
18	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
19	lnc-SLC35G4-1	chr18:11503733-11503935	XLOC_012626
20	lnc-SLC35G4-1	chr18:11505775-11505923	XLOC_012626
21	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
22	lnc-SLC35G4-1	chr18:11506531-11506635	ENSG00000267252.1
23	lnc-SLC35G4-1	chr18:11506531-11506635	NONHSAT057308
24	lnc-SLC35G4-1	chr18:11506531-11506635	XLOC_012626
25	lnc-SLC35G4-1	chr18:11505502-11506635	NONHSAT057314

Variant related genes	Relation type
ENSG00000267252	TF binding region
NUP153	miRNA target sites
TMEM9B	miRNA target sites
SLC30A7	miRNA target sites
TMF1	miRNA target sites

Extended variants
information (count: 335 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs732872	chr18:11502864-11502865	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186298904	chr18:11502884-11502885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs732871	chr18:11502894-11502895	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs373798425	chr18:11502898-11502899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs732870	chr18:11502908-11502909	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs569576441	chr18:11503007-11503008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539731423	chr18:11503008-11503009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557766025	chr18:11503028-11503029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79888273	chr18:11503032-11503033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577988478	chr18:11503039-11503040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189468869	chr18:11503068-11503069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141163993	chr18:11503121-11503122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78357403	chr18:11503179-11503180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573881973	chr18:11503256-11503257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544464613	chr18:11503311-11503312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs8093677	chr18:11503332-11503333	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs577901767	chr18:11503356-11503357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544952387	chr18:11503357-11503358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564526419	chr18:11503368-11503369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528428724	chr18:11503417-11503418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs8094650	chr18:11503451-11503452	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs561893662	chr18:11503452-11503453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79193032	chr18:11503457-11503458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs8093875	chr18:11503484-11503485	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs138754640	chr18:11503488-11503489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569332693	chr18:11503495-11503496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201669359	chr18:11503497-11503498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9961424	chr18:11503512-11503513	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs7238494	chr18:11503547-11503548	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs139716100	chr18:11503565-11503566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200792117	chr18:11503570-11503571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533720146	chr18:11503584-11503585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111884142	chr18:11503591-11503592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201708312	chr18:11503600-11503601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537554011	chr18:11503628-11503629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200686061	chr18:11503629-11503630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572695620	chr18:11503630-11503631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190900996	chr18:11503641-11503642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10676913	chr18:11503651-11503652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs33919178	chr18:11503652-11503653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs386387071	chr18:11503653-11503654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs397741252	chr18:11503656-11503657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532835998	chr18:11503665-11503666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115995547	chr18:11503678-11503679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186516449	chr18:11503697-11503698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114581384	chr18:11503709-11503710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551415498	chr18:11503781-11503782	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs191673411	chr18:11503789-11503790	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs75316631	chr18:11503790-11503791	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs8094064	chr18:11503802-11503803	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:57)

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
abnormal development	18461090	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	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11500200-11506600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:11501000-11505800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr18:11501600-11504000	Enhancers	HepG2	liver
4	chr18:11502000-11506400	Weak transcription	Hela-S3	cervix
5	chr18:11502600-11506600	Weak transcription	NH-A	brain
6	chr18:11502600-11513200	Weak transcription	NHDF-Ad	bronchial
7	chr18:11503000-11503400	Enhancers	Thymus	Thymus
8	chr18:11503200-11504400	Enhancers	Fetal Thymus	thymus
9	chr18:11503400-11503800	Weak transcription	Thymus	Thymus
10	chr18:11503800-11504000	Enhancers	Thymus	Thymus
11	chr18:11504000-11504800	Weak transcription	Thymus	Thymus
12	chr18:11504400-11504800	Weak transcription	Fetal Thymus	thymus
13	chr18:11504800-11507000	Enhancers	Fetal Thymus	thymus
14	chr18:11504800-11507000	Enhancers	Thymus	Thymus
15	chr18:11504800-11507200	Enhancers	Dnd41	blood
16	chr18:11505800-11506200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr18:11506400-11507400	Enhancers	Hela-S3	cervix
18	chr18:11506600-11506800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr18:11506600-11506800	Enhancers	Osteobl	bone
20	chr18:11506600-11507000	Enhancers	NH-A	brain
21	chr18:11506800-11507000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr18:11506800-11507000	Flanking Active TSS	Osteobl	bone
23	chr18:11507000-11507200	Enhancers	Osteobl	bone
24	chr18:11507000-11509800	Weak transcription	Fetal Thymus	thymus
25	chr18:11507000-11511800	Weak transcription	Thymus	Thymus
26	chr18:11507200-11509000	Weak transcription	Dnd41	blood
27	chr18:11507400-11512000	Weak transcription	Hela-S3	cervix
28	chr18:11509000-11511800	Enhancers	Dnd41	blood
29	chr18:11509800-11511800	Enhancers	Fetal Thymus	thymus

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