Variant report

Variant	nsv2209
Chromosome Location	chr18:13276410-13316570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:13290891-13291099	HepG2	liver:	n/a	n/a
2	ATF2	chr18:13288745-13289077	GM12878	blood:	n/a	n/a
3	ATF2	chr18:13279417-13279791	GM12878	blood:	n/a	n/a
4	BATF	chr18:13290825-13291251	GM12878	blood:	n/a	chr18:13291193-13291206
5	BATF	chr18:13288528-13289098	GM12878	blood:	n/a	n/a
6	BATF	chr18:13288604-13289075	GM12878	blood:	n/a	n/a
7	BATF	chr18:13289530-13289752	GM12878	blood:	n/a	chr18:13289634-13289644 chr18:13289638-13289648 chr18:13289633-13289644
8	BATF	chr18:13279522-13279792	GM12878	blood:	n/a	chr18:13279543-13279551
9	BCL11A	chr18:13279222-13279711	GM12878	blood:	n/a	chr18:13279320-13279328
10	BCL11A	chr18:13288551-13288761	GM12878	blood:	n/a	n/a
11	BCL11A	chr18:13288536-13289073	GM12878	blood:	n/a	n/a
12	BHLHE40	chr18:13313072-13313354	HepG2	liver:	n/a	chr18:13313242-13313263 chr18:13313249-13313258
13	BHLHE40	chr18:13313143-13313337	K562	blood:	n/a	chr18:13313242-13313263 chr18:13313249-13313258
14	BHLHE40	chr18:13312893-13313552	HepG2	liver:	n/a	chr18:13313242-13313263 chr18:13313249-13313258
15	BHLHE40	chr18:13279347-13279403	GM12878	blood:	n/a	n/a
16	BHLHE40	chr18:13288758-13288958	GM12878	blood:	n/a	n/a
17	CBX3	chr18:13316040-13316361	K562	blood:	n/a	n/a
18	CBX3	chr18:13316097-13316399	K562	blood:	n/a	n/a
19	CHD2	chr18:13283821-13284154	K562	blood:	n/a	n/a
20	CHD2	chr18:13279277-13279591	GM12878	blood:	n/a	n/a
21	CTCF	chr18:13302500-13302650	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr18:13302580-13302730	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr18:13303040-13303190	WERI-Rb-1	eye:	n/a	chr18:13303119-13303132
24	CTCF	chr18:13287460-13287610	Caco-2	colon:	n/a	n/a
25	CTCF	chr18:13277220-13277370	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr18:13298540-13298690	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr18:13307690-13307751	GM20000	blood:	n/a	n/a
28	CTCF	chr18:13303073-13303216	H1-hESC	embryonic stem cell:	n/a	chr18:13303119-13303132
29	CTCF	chr18:13287500-13287650	HEK293	kidney:	n/a	n/a
30	CTCF	chr18:13303080-13303230	GM12873	blood:	n/a	chr18:13303119-13303132
31	CTCF	chr18:13287547-13287591	K562	blood:	n/a	n/a
32	CTCF	chr18:13302540-13302690	AG04449	skin:	n/a	n/a
33	CTCF	chr18:13302600-13302750	MCF-7	breast:	n/a	n/a
34	CTCF	chr18:13309356-13309357	K562	blood:	n/a	n/a
35	CTCF	chr18:13313656-13313701	LNCaP	prostate:	n/a	n/a
36	CTCF	chr18:13277180-13277330	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr18:13298626-13298686	GM20000	blood:	n/a	n/a
38	CTCF	chr18:13302600-13302750	AG10803	skin:	n/a	n/a
39	CTCF	chr18:13302580-13302730	AG10803	skin:	n/a	n/a
40	CTCF	chr18:13303087-13303136	LNCaP	prostate:	n/a	chr18:13303119-13303132
41	CTCF	chr18:13303120-13303270	GM12875	blood:	n/a	n/a
42	CTCF	chr18:13287530-13287606	MCF-7	breast:	n/a	n/a
43	CTCF	chr18:13303100-13303250	HEK293	kidney:	n/a	chr18:13303119-13303132
44	CTCF	chr18:13287480-13287630	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr18:13303060-13303210	HEK293	kidney:	n/a	chr18:13303119-13303132
46	CTCF	chr18:13302500-13302650	GM12873	blood:	n/a	n/a
47	CTCF	chr18:13287540-13287624	Medullo	brain:	n/a	n/a
48	CTCF	chr18:13302500-13302650	MCF-7	breast:	n/a	n/a
49	CTCF	chr18:13287507-13287638	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr18:13287533-13287625	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:13300968-13301018	HCPEpiC	choroid plexus:	n/a
2	chr18:13300968-13301018	AG09319	gingival:	n/a
3	chr18:13300968-13301018	Hela-S3	cervix:	n/a
4	chr18:13300968-13301018	AG10803	skin:	n/a
5	chr18:13300968-13301018	GM12892	blood:	n/a
6	chr18:13300968-13301018	HIPEpiC	eye:	n/a
7	chr18:13300968-13301018	BJ	skin:	n/a
8	chr18:13300968-13301018	HRPEpiC	eye:	n/a
9	chr18:13300968-13301018	SK-N-SH_RA	brain:	n/a
10	chr18:13300968-13301018	ProgFib	skin:	n/a
11	chr18:13300968-13301018	SK-N-SH	brain:	n/a
12	chr18:13300968-13301018	GM06990	blood:	n/a
13	chr18:13300968-13301018	GM12891	blood:	n/a
14	chr18:13300968-13301018	ECC-1	luminal epithelium:	n/a
15	chr18:13300968-13301018	H1-hESC	embryonic stem cell:	embryo
16	chr18:13300968-13301018	SK-N-MC	brain:	n/a
17	chr18:13300968-13301018	NT2-D1	testis:	n/a
18	chr18:13300968-13301018	PANC-1	pancreas:	n/a
19	chr18:13300968-13301018	AG04450	lung:	fetal
20	chr18:13300968-13301018	HAEpiC	amniotic membrane:	n/a
21	chr18:13300968-13301018	HRCEpiC	kidney:	n/a
22	chr18:13300968-13301018	NH-A	brain:	n/a
23	chr18:13300968-13301018	HEK293	kidney:	embryo
24	chr18:13300968-13301018	K562	blood:	n/a
25	chr18:13300968-13301018	Caco-2	colon:	n/a
26	chr18:13300968-13301018	A549	lung:	n/a
27	chr18:13300968-13301018	HEEpiC	esophagus:	n/a
28	chr18:13300968-13301018	NHDF-neo	bronchial:	n/a
29	chr18:13300968-13301018	LNCaP	prostate:	n/a
30	chr18:13300968-13301018	MCF10A-Er-Src	breast:	n/a
31	chr18:13300968-13301018	ovcar-3	ovarian:	n/a
32	chr18:13300968-13301018	HMEC	breast:	n/a
33	chr18:13300968-13301018	T-47D	breast:	n/a
34	chr18:13300968-13301018	IMR90	lung:	fetal
35	chr18:13300968-13301018	U87	brain:	n/a
36	chr18:13300968-13301018	AG04449	skin:	fetal
37	chr18:13300968-13301018	MCF-7	breast:	n/a
38	chr18:13300968-13301018	AoSMC	blood vessel:	n/a
39	chr18:13300968-13301018	NHBE	bronchial:	n/a
40	chr18:13300968-13301018	HUVEC	blood vessel:	n/a
41	chr18:13300968-13301018	PFSK-1	brain:	n/a
42	chr18:13300968-13301018	HRE	kidney:	n/a
43	chr18:13300968-13301018	HL-60	blood:	n/a
44	chr18:13300968-13301018	CMK	blood:	n/a
45	chr18:13300968-13301018	HPAEpiC	pulmonary alveolar:	n/a
46	chr18:13300968-13301018	BE2_C	brain:	n/a
47	chr18:13300968-13301018	NB4	blood:	n/a
48	chr18:13300968-13301018	HCM	heart:	n/a
49	chr18:13300968-13301018	GM19239	blood:	n/a
50	chr18:13300968-13301018	HepG2	liver:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:13286921..13290760-chr18:13293338..13296944,6	MCF-7	breast:
2	chr18:13286921..13290760-chr18:13293338..13296944,6	MCF-7	breast:
3	chr18:13313464..13315370-chr18:13333463..13336415,2	MCF-7	breast:
4	chr18:13293376..13296291-chr18:13300592..13303207,3	MCF-7	breast:
5	chr18:13217515..13220482-chr18:13305759..13307336,2	MCF-7	breast:
6	chr18:13283569..13285472-chr18:13287547..13289155,2	MCF-7	breast:
7	chr18:13265432..13267712-chr18:13286156..13288940,2	MCF-7	breast:
8	chr18:13215610..13217776-chr18:13298928..13300832,2	MCF-7	breast:
9	chr18:13286615..13289389-chr18:13302517..13304559,2	MCF-7	breast:
10	chr18:13286615..13289389-chr18:13302517..13304559,2	MCF-7	breast:
11	chr18:13266595..13268612-chr18:13295216..13296927,2	MCF-7	breast:
12	chr18:13283569..13285472-chr18:13287547..13289155,2	MCF-7	breast:
13	chr18:13297804..13299921-chr18:13302909..13305321,2	MCF-7	breast:
14	chr18:13276824..13278718-chr18:13280381..13284195,3	MCF-7	breast:
15	chr18:13284936..13285757-chr18:13394689..13395619,3	MCF-7	breast:
16	chr18:13293376..13296291-chr18:13300592..13303207,3	MCF-7	breast:
17	chr18:13291375..13292050-chr8:53976127..53977109,2	MCF-7	breast:
18	chr18:13297804..13299921-chr18:13302909..13305321,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C18orf1-1	chr18:13278104-13278187	NONHSAT058420
2	lnc-C18orf1-1	chr18:13278104-13278375	NONHSAT058421

No data

Variant related genes	Relation type
LDLRAD4	TF binding region
LDLRAD4	CpG island
ENSG00000267239	chromatin interactions
ENSG00000168675	chromatin interactions

Extended variants
information (count: 1591 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181247525	chr18:13276429-13276430	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs569650315	chr18:13276431-13276432	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs185073959	chr18:13276606-13276607	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs36050242	chr18:13276622-13276623	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs77307742	chr18:13276628-13276629	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs115665586	chr18:13276668-13276669	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs540630507	chr18:13276680-13276681	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs553077627	chr18:13276717-13276718	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs114002200	chr18:13276718-13276719	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs543275691	chr18:13276741-13276742	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs561441524	chr18:13276782-13276783	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs141939251	chr18:13276834-13276835	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544110226	chr18:13276846-13276847	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565398266	chr18:13276907-13276908	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532540031	chr18:13276908-13276909	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563175345	chr18:13276926-13276927	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547473887	chr18:13276927-13276928	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559838472	chr18:13276933-13276934	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376404126	chr18:13276998-13276999	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs530119068	chr18:13277018-13277019	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs145730605	chr18:13277135-13277136	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs569539206	chr18:13277165-13277166	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs189589823	chr18:13277215-13277216	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs115224145	chr18:13277218-13277219	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs570610476	chr18:13277307-13277308	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs534651808	chr18:13277340-13277341	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs56078702	chr18:13277341-13277342	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs574609847	chr18:13277350-13277351	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs181472658	chr18:13277378-13277379	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs142843978	chr18:13277381-13277382	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs576719039	chr18:13277383-13277384	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs567269652	chr18:13277391-13277392	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs76666374	chr18:13277401-13277402	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs577459233	chr18:13277405-13277406	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs541450082	chr18:13277411-13277412	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs78449150	chr18:13277418-13277419	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs372060199	chr18:13277424-13277425	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs374964200	chr18:13277466-13277467	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs76238120	chr18:13277471-13277472	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs147407107	chr18:13277573-13277574	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs59949510	chr18:13277574-13277575	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs571287479	chr18:13277579-13277580	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs118019060	chr18:13277606-13277607	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552075315	chr18:13277627-13277628	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570755920	chr18:13277664-13277665	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368803394	chr18:13277671-13277672	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556692357	chr18:13277705-13277706	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7227136	chr18:13277724-13277725	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546842509	chr18:13277752-13277753	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568078619	chr18:13277832-13277833	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	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
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	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
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:945 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:13243600-13278200	Weak transcription	Dnd41	blood
2	chr18:13259200-13280000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr18:13261200-13282200	Weak transcription	Small Intestine	intestine
4	chr18:13268400-13276800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr18:13268600-13276600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr18:13269400-13280000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr18:13270000-13276600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr18:13270000-13276800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr18:13270000-13279200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr18:13270000-13279800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr18:13270000-13283800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr18:13270000-13290000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr18:13270200-13278400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr18:13270200-13284600	Weak transcription	Psoas Muscle	Psoas
15	chr18:13270200-13288200	Weak transcription	Fetal Intestine Large	intestine
16	chr18:13270200-13290200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr18:13270200-13297600	Weak transcription	Colonic Mucosa	Colon
18	chr18:13270400-13279600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr18:13270800-13279000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr18:13270800-13279800	Weak transcription	Adipose Nuclei	Adipose
21	chr18:13270800-13282600	Weak transcription	Fetal Intestine Small	intestine
22	chr18:13271400-13281600	Weak transcription	Brain Germinal Matrix	brain
23	chr18:13271800-13276600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr18:13271800-13278600	Weak transcription	Liver	Liver
25	chr18:13272800-13284800	Weak transcription	Esophagus	oesophagus
26	chr18:13272800-13289600	Weak transcription	Gastric	stomach
27	chr18:13273200-13283800	Weak transcription	Spleen	Spleen
28	chr18:13274000-13276600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr18:13274000-13279000	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr18:13274200-13276600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr18:13274200-13279000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr18:13274400-13276600	Weak transcription	Fetal Brain Male	brain
33	chr18:13274400-13277200	Weak transcription	Pancreas	Pancrea
34	chr18:13274400-13277400	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr18:13274400-13277800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr18:13274400-13278000	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr18:13274400-13278400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr18:13274400-13279000	Weak transcription	Fetal Kidney	kidney
39	chr18:13274400-13279200	Enhancers	Primary T cells from cord blood	blood
40	chr18:13274600-13278800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr18:13274600-13278800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr18:13274600-13282400	Weak transcription	HepG2	liver
43	chr18:13274600-13284000	Weak transcription	Rectal Smooth Muscle	rectum
44	chr18:13274600-13284200	Weak transcription	Colon Smooth Muscle	Colon
45	chr18:13274600-13301600	Weak transcription	Brain Substantia Nigra	brain
46	chr18:13274600-13302400	Weak transcription	Primary hematopoietic stem cells	blood
47	chr18:13275800-13276600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr18:13275800-13276800	Enhancers	Fetal Thymus	thymus
49	chr18:13275800-13277000	Enhancers	Thymus	Thymus
50	chr18:13275800-13278800	Weak transcription	Primary B cells from cord blood	blood

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