Variant report

Variant	nsv132152
Chromosome Location	chr18:12885273-12890021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:311)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:12885459-12885677	K562	blood:	n/a	n/a
2	ATF2	chr18:12885468-12886010	GM12878	blood:	n/a	n/a
3	ATF2	chr18:12885496-12885957	GM12878	blood:	n/a	n/a
4	BCL11A	chr18:12885586-12885970	GM12878	blood:	n/a	chr18:12885621-12885629
5	BHLHE40	chr18:12885061-12885968	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:12886663-12886735	GM12878	blood:	n/a	n/a
7	CBX3	chr18:12886461-12886980	HCT-116	colon:	n/a	n/a
8	CCNT2	chr18:12885423-12885668	K562	blood:	n/a	chr18:12885541-12885561
9	CEBPB	chr18:12889941-12890689	Hela-S3	cervix:	n/a	n/a
10	CEBPD	chr18:12885350-12885779	K562	blood:	n/a	n/a
11	CHD1	chr18:12884493-12885656	GM12878	blood:	n/a	n/a
12	CHD2	chr18:12885500-12885944	GM12878	blood:	n/a	n/a
13	CTCF	chr18:12886680-12886830	NHEK	skin:	n/a	n/a
14	CTCF	chr18:12886660-12886810	GM12872	blood:	n/a	n/a
15	CTCF	chr18:12886594-12886830	HepG2	liver:	n/a	n/a
16	CTCF	chr18:12886640-12886790	AG04449	skin:	n/a	n/a
17	CTCF	chr18:12886620-12886770	HepG2	liver:	n/a	n/a
18	CTCF	chr18:12886640-12886790	GM12868	blood:	n/a	n/a
19	CTCF	chr18:12886547-12886901	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr18:12886640-12886790	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr18:12886529-12886863	LNCaP	prostate:	n/a	n/a
22	CTCF	chr18:12886620-12886770	GM06990	blood:	n/a	n/a
23	CTCF	chr18:12886700-12886850	K562	blood:	n/a	n/a
24	CTCF	chr18:12886378-12887005	A549	lung:	n/a	n/a
25	CTCF	chr18:12886641-12886848	MCF-7	breast:	n/a	n/a
26	CTCF	chr18:12886620-12886770	HCM	heart:	n/a	n/a
27	CTCF	chr18:12886680-12886830	NB4	blood:	n/a	n/a
28	CTCF	chr18:12886533-12886805	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr18:12886580-12886730	MCF-7	breast:	n/a	n/a
30	CTCF	chr18:12886640-12886790	HPF	lung:	n/a	n/a
31	CTCF	chr18:12886680-12886830	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr18:12886360-12886510	GM12872	blood:	n/a	n/a
33	CTCF	chr18:12886840-12886990	A549	lung:	n/a	n/a
34	CTCF	chr18:12886637-12886812	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr18:12886578-12886873	HepG2	liver:	n/a	n/a
36	CTCF	chr18:12886640-12886790	GM12865	blood:	n/a	n/a
37	CTCF	chr18:12886620-12886770	AG09319	gingival:	n/a	n/a
38	CTCF	chr18:12886680-12886830	HVMF	connective:	n/a	n/a
39	CTCF	chr18:12886660-12886810	HPF	lung:	n/a	n/a
40	CTCF	chr18:12886620-12886770	BE2_C	brain:	n/a	n/a
41	CTCF	chr18:12886640-12886790	HL-60	blood:	n/a	n/a
42	CTCF	chr18:12886680-12886830	AG04450	lung:	n/a	n/a
43	CTCF	chr18:12886640-12886790	MCF-7	breast:	n/a	n/a
44	CTCF	chr18:12886760-12886910	HAc	cerebellar:	n/a	n/a
45	CTCF	chr18:12886620-12886770	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr18:12886680-12886830	GM12864	blood:	n/a	n/a
47	CTCF	chr18:12886680-12886830	GM06990	blood:	n/a	n/a
48	CTCF	chr18:12886785-12886812	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr18:12886620-12886770	BJ	skin:	n/a	n/a
50	CTCF	chr18:12886540-12886690	GM12870	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12885569-12885619	AG10803	skin:	n/a
2	chr18:12887356-12887406	AG04450	lung:	fetal
3	chr18:12887356-12887406	AG10803	skin:	n/a
4	chr18:12887356-12887406	HEEpiC	esophagus:	n/a
5	chr18:12885569-12885619	Jurkat	blood:	n/a
6	chr18:12887356-12887406	GM12878	blood:	n/a
7	chr18:12885569-12885619	HEEpiC	esophagus:	n/a
8	chr18:12885569-12885619	LNCaP	prostate:	n/a
9	chr18:12885569-12885619	AoSMC	blood vessel:	n/a
10	chr18:12885569-12885619	A549	lung:	n/a
11	chr18:12887356-12887406	BE2_C	brain:	n/a
12	chr18:12887356-12887406	SAEC	small airway:	n/a
13	chr18:12885569-12885619	T-47D	breast:	n/a
14	chr18:12887356-12887406	CMK	blood:	n/a
15	chr18:12885569-12885619	HRCEpiC	kidney:	n/a
16	chr18:12887356-12887406	GM12892	blood:	n/a
17	chr18:12887356-12887406	SK-N-SH_RA	brain:	n/a
18	chr18:12885569-12885619	AG09319	gingival:	n/a
19	chr18:12885569-12885619	SK-N-SH	brain:	n/a
20	chr18:12887356-12887406	HCM	heart:	n/a
21	chr18:12887356-12887406	T-47D	breast:	n/a
22	chr18:12885569-12885619	SK-N-MC	brain:	n/a
23	chr18:12887356-12887406	MCF10A-Er-Src	breast:	n/a
24	chr18:12887356-12887406	NHBE	bronchial:	n/a
25	chr18:12885569-12885619	AG09309	skin:	n/a
26	chr18:12887356-12887406	Caco-2	colon:	n/a
27	chr18:12887356-12887406	RPTEC	kidney:	n/a
28	chr18:12885569-12885619	HIPEpiC	eye:	n/a
29	chr18:12887356-12887406	PANC-1	pancreas:	n/a
30	chr18:12887356-12887406	HAEpiC	amniotic membrane:	n/a
31	chr18:12887356-12887406	Jurkat	blood:	n/a
32	chr18:12887356-12887406	AG09309	skin:	n/a
33	chr18:12887356-12887406	HRCEpiC	kidney:	n/a
34	chr18:12885569-12885619	U87	brain:	n/a
35	chr18:12885569-12885619	PrEC	prostate:	n/a
36	chr18:12885569-12885619	ProgFib	skin:	n/a
37	chr18:12887356-12887406	NH-A	brain:	n/a
38	chr18:12887356-12887406	IMR90	lung:	fetal
39	chr18:12887356-12887406	NB4	blood:	n/a
40	chr18:12885569-12885619	NHDF-neo	bronchial:	n/a
41	chr18:12887356-12887406	BJ	skin:	n/a
42	chr18:12887356-12887406	Hela-S3	cervix:	n/a
43	chr18:12885569-12885619	PANC-1	pancreas:	n/a
44	chr18:12885569-12885619	CMK	blood:	n/a
45	chr18:12887356-12887406	HepG2	liver:	n/a
46	chr18:12885569-12885619	RPTEC	kidney:	n/a
47	chr18:12887356-12887406	K562	blood:	n/a
48	chr18:12887356-12887406	HCF	heart:	n/a
49	chr18:12885569-12885619	Hela-S3	cervix:	n/a
50	chr18:12885569-12885619	NH-A	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12720578..12722962-chr18:12886725..12888628,2	MCF-7	breast:
2	chr18:12882771..12885367-chr18:12946819..12949664,2	MCF-7	breast:
3	chr18:12725367..12727823-chr18:12887215..12889210,2	K562	blood:
4	chr18:12880282..12885478-chr18:12946145..12950206,8	K562	blood:
5	chr15:65596946..65598700-chr18:12882626..12885488,2	MCF-7	breast:
6	chr18:12845560..12847901-chr18:12888541..12891505,2	MCF-7	breast:
7	chr18:12885210..12887915-chr18:12922240..12924261,2	K562	blood:
8	chr18:12881929..12887234-chr18:12887997..12891131,8	MCF-7	breast:
9	chr18:12884698..12887915-chr18:12921814..12925737,3	K562	blood:
10	chr18:12774117..12776643-chr18:12883699..12885836,3	K562	blood:
11	chr18:12760116..12762309-chr18:12883836..12885442,2	K562	blood:
12	chr18:12889378..12891931-chr18:12911330..12913898,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEH1L-5	chr18:12884514-12885555	NONHSAT058399

No data

Variant related genes	Relation type
PTPN2	TF binding region
PTPN2	CpG island
ENSG00000085415	chromatin interactions
ENSG00000260302	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000267336	chromatin interactions
ENSG00000175354	chromatin interactions
ENSG00000201466	chromatin interactions

Extended variants
information (count: 197 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:197 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77959050	chr18:12885273-12885274	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
2	rs556500686	chr18:12885280-12885281	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
3	rs571280040	chr18:12885286-12885287	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs538664978	chr18:12885297-12885298	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
5	rs553810664	chr18:12885299-12885300	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
6	rs572212141	chr18:12885309-12885310	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs536447063	chr18:12885337-12885338	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs180818808	chr18:12885399-12885400	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs576261471	chr18:12885419-12885420	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs185418444	chr18:12885435-12885436	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs148555706	chr18:12885461-12885462	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs576864895	chr18:12885480-12885481	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs191400952	chr18:12885502-12885503	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs183157036	chr18:12885551-12885552	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs188288292	chr18:12885559-12885560	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs142909392	chr18:12885568-12885569	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs561351727	chr18:12885574-12885575	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs35923716	chr18:12885577-12885578	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112947592	chr18:12885590-12885591	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs142390800	chr18:12885600-12885601	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs116376932	chr18:12885620-12885621	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538603487	chr18:12885650-12885651	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs191391875	chr18:12885652-12885653	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs565829585	chr18:12885715-12885716	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536383463	chr18:12885721-12885722	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs76060221	chr18:12885725-12885726	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs145031775	chr18:12885729-12885730	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147562242	chr18:12885737-12885738	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558840795	chr18:12885755-12885756	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs8087077	chr18:12885809-12885810	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs543934498	chr18:12885821-12885822	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113677093	chr18:12885826-12885827	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs574452291	chr18:12885827-12885828	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541532271	chr18:12885885-12885886	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs45524731	chr18:12885902-12885903	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563547060	chr18:12885925-12885926	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs113252814	chr18:12885955-12885956	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs150163274	chr18:12886043-12886044	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs138606888	chr18:12886059-12886060	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs371521251	chr18:12886070-12886071	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs550353847	chr18:12886092-12886093	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs183756731	chr18:12886093-12886094	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532710323	chr18:12886115-12886116	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs3809915	chr18:12886163-12886164	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs143531406	chr18:12886176-12886177	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs565175657	chr18:12886178-12886179	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs536663256	chr18:12886215-12886216	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs549270118	chr18:12886221-12886222	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs548350935	chr18:12886350-12886351	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs45576131	chr18:12886373-12886374	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

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

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12882400-12885600	Active TSS	Breast Myoepithelial Primary Cells	Breast
2	chr18:12883200-12885600	Active TSS	Rectal Mucosa Donor 29	rectum
3	chr18:12883800-12885400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr18:12884600-12885400	Flanking Active TSS	Primary B cells from cord blood	blood
5	chr18:12884600-12885400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
6	chr18:12884600-12885400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr18:12884600-12885600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr18:12884600-12885600	Flanking Active TSS	Fetal Thymus	thymus
9	chr18:12884600-12885800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr18:12884800-12885400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr18:12884800-12885400	Flanking Active TSS	NHEK	skin
12	chr18:12884800-12885600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr18:12884800-12885600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr18:12884800-12885600	Weak transcription	Psoas Muscle	Psoas
15	chr18:12884800-12885600	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr18:12884800-12885600	Flanking Active TSS	K562	blood
17	chr18:12884800-12886000	Enhancers	Small Intestine	intestine
18	chr18:12884800-12886400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr18:12885000-12885400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr18:12885000-12885400	Enhancers	Liver	Liver
21	chr18:12885000-12885400	Enhancers	Colon Smooth Muscle	Colon
22	chr18:12885000-12885400	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr18:12885000-12885400	Enhancers	Fetal Brain Male	brain
24	chr18:12885000-12885400	Enhancers	Fetal Brain Female	brain
25	chr18:12885000-12885400	Enhancers	Stomach Smooth Muscle	stomach
26	chr18:12885000-12885400	Flanking Active TSS	Thymus	Thymus
27	chr18:12885000-12885400	Flanking Active TSS	HMEC	breast
28	chr18:12885000-12885600	Enhancers	Primary T cells from cord blood	blood
29	chr18:12885000-12885600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr18:12885000-12885600	Enhancers	Brain Angular Gyrus	brain
31	chr18:12885000-12885600	Enhancers	Dnd41	blood
32	chr18:12885000-12885800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr18:12885000-12885800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr18:12885000-12885800	Enhancers	Stomach Mucosa	stomach
35	chr18:12885000-12885800	Enhancers	HepG2	liver
36	chr18:12885000-12886000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr18:12885000-12886000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr18:12885000-12886000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr18:12885000-12886000	Flanking Active TSS	GM12878-XiMat	blood
40	chr18:12885000-12886600	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr18:12885000-12886800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr18:12885000-12887000	Enhancers	H1 Cell Line	embryonic stem cell
43	chr18:12885000-12887400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr18:12885000-12888600	Weak transcription	Fetal Stomach	stomach
45	chr18:12885200-12885400	Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr18:12885200-12885400	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr18:12885200-12885400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr18:12885200-12885400	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr18:12885200-12885400	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr18:12885200-12885400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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