Variant report

Variant	esv3436965
Chromosome Location	chr18:12420352-12421500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:375)
CpG islands
(count:183)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:12421215-12421460	HepG2	liver:	n/a	n/a
2	BACH1	chr18:12419896-12420532	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:12421133-12421470	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr18:12420897-12421455	HepG2	liver:	n/a	n/a
5	BHLHE40	chr18:12420957-12421323	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:12420274-12420589	GM12878	blood:	n/a	chr18:12420275-12420291 chr18:12420498-12420514
7	BRCA1	chr18:12420393-12420404	GM12878	blood:	n/a	n/a
8	BRCA1	chr18:12421213-12421326	HepG2	liver:	n/a	n/a
9	BRCA1	chr18:12421140-12421360	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr18:12420233-12420411	HepG2	liver:	n/a	n/a
11	CCNT2	chr18:12420365-12420500	K562	blood:	n/a	n/a
12	CEBPD	chr18:12420920-12421405	HepG2	liver:	n/a	n/a
13	CEBPD	chr18:12420264-12420519	HepG2	liver:	n/a	n/a
14	CHD1	chr18:12420310-12420471	GM12878	blood:	n/a	n/a
15	CHD1	chr18:12420951-12421704	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr18:12420026-12420374	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr18:12420958-12421341	GM12878	blood:	n/a	n/a
18	CHD2	chr18:12420158-12420501	HepG2	liver:	n/a	n/a
19	CHD2	chr18:12420969-12421099	HepG2	liver:	n/a	n/a
20	CHD2	chr18:12420304-12420532	GM12878	blood:	n/a	n/a
21	CHD2	chr18:12419978-12420459	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr18:12419890-12420560	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr18:12420970-12421204	GM12878	blood:	n/a	n/a
24	CHD2	chr18:12420864-12421173	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr18:12420320-12420470	GM12873	blood:	n/a	n/a
26	CTCF	chr18:12420354-12420482	GM10248	blood:	n/a	n/a
27	CTCF	chr18:12420363-12420472	MCF-7	breast:	n/a	n/a
28	CTCF	chr18:12420300-12420450	GM12865	blood:	n/a	n/a
29	CTCF	chr18:12420380-12420530	SAEC	small airway:	n/a	n/a
30	CTCF	chr18:12420822-12421303	H1-hESC	embryonic stem cell:	n/a	chr18:12421108-12421116 chr18:12421161-12421174 chr18:12421101-12421119
31	CTCF	chr18:12420240-12420390	GM12875	blood:	n/a	n/a
32	CTCF	chr18:12420280-12420430	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr18:12420363-12420462	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr18:12421320-12421470	HepG2	liver:	n/a	chr18:12421367-12421375
35	CTCF	chr18:12420260-12420410	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr18:12420340-12420490	AG09319	gingival:	n/a	n/a
37	CTCF	chr18:12420300-12420450	HFF	foreskin:	n/a	n/a
38	CTCF	chr18:12420340-12420490	GM12869	blood:	n/a	n/a
39	CTCF	chr18:12420320-12420470	GM12870	blood:	n/a	n/a
40	CTCF	chr18:12420300-12420450	GM12864	blood:	n/a	n/a
41	CTCF	chr18:12420332-12420494	MCF-7	breast:	n/a	n/a
42	CTCF	chr18:12420260-12420410	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr18:12421100-12421250	GM12874	blood:	n/a	chr18:12421108-12421116 chr18:12421161-12421174 chr18:12421101-12421119
44	CTCF	chr18:12420320-12420470	HepG2	liver:	n/a	n/a
45	CTCF	chr18:12420220-12420370	GM12867	blood:	n/a	n/a
46	CTCF	chr18:12420300-12420450	AG09319	gingival:	n/a	n/a
47	CTCF	chr18:12420220-12420370	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr18:12420300-12420450	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr18:12420240-12420390	HRE	kidney:	n/a	n/a
50	CTCF	chr18:12420360-12420510	GM12871	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12420412-12420462	HIPEpiC	eye:	n/a
2	chr18:12420412-12420462	NH-A	brain:	n/a
3	chr18:12420412-12420462	HAEpiC	amniotic membrane:	n/a
4	chr18:12420412-12420462	HCF	heart:	n/a
5	chr18:12420412-12420462	HRE	kidney:	n/a
6	chr18:12420862-12420912	H1-hESC	embryonic stem cell:	embryo
7	chr18:12420412-12420462	AG10803	skin:	n/a
8	chr18:12420412-12420462	SK-N-SH	brain:	n/a
9	chr18:12421072-12421122	SK-N-SH_RA	brain:	n/a
10	chr18:12420412-12420462	MCF10A-Er-Src	breast:	n/a
11	chr18:12420862-12420912	HRE	kidney:	n/a
12	chr18:12420862-12420912	SAEC	small airway:	n/a
13	chr18:12420412-12420462	MCF-7	breast:	n/a
14	chr18:12420862-12420912	HCT-116	colon:	n/a
15	chr18:12420412-12420462	PANC-1	pancreas:	n/a
16	chr18:12420412-12420462	K562	blood:	n/a
17	chr18:12420412-12420462	HRPEpiC	eye:	n/a
18	chr18:12421072-12421122	HMEC	breast:	n/a
19	chr18:12421072-12421122	HRPEpiC	eye:	n/a
20	chr18:12420412-12420462	GM12891	blood:	n/a
21	chr18:12420412-12420462	NHDF-neo	bronchial:	n/a
22	chr18:12421072-12421122	AG09319	gingival:	n/a
23	chr18:12421072-12421122	Jurkat	blood:	n/a
24	chr18:12420862-12420912	AG04449	skin:	fetal
25	chr18:12420412-12420462	PFSK-1	brain:	n/a
26	chr18:12421072-12421122	LNCaP	prostate:	n/a
27	chr18:12421072-12421122	ovcar-3	ovarian:	n/a
28	chr18:12421072-12421122	A549	lung:	n/a
29	chr18:12421072-12421122	MCF10A-Er-Src	breast:	n/a
30	chr18:12420412-12420462	HCT-116	colon:	n/a
31	chr18:12420412-12420462	HCPEpiC	choroid plexus:	n/a
32	chr18:12420862-12420912	NB4	blood:	n/a
33	chr18:12421072-12421122	NHBE	bronchial:	n/a
34	chr18:12421072-12421122	SK-N-MC	brain:	n/a
35	chr18:12421072-12421122	IMR90	lung:	fetal
36	chr18:12420412-12420462	GM12892	blood:	n/a
37	chr18:12421072-12421122	HAEpiC	amniotic membrane:	n/a
38	chr18:12421072-12421122	HRE	kidney:	n/a
39	chr18:12421072-12421122	AG04449	skin:	fetal
40	chr18:12420862-12420912	AG04450	lung:	fetal
41	chr18:12420412-12420462	HCM	heart:	n/a
42	chr18:12420412-12420462	GM19239	blood:	n/a
43	chr18:12420862-12420912	PANC-1	pancreas:	n/a
44	chr18:12420862-12420912	HCF	heart:	n/a
45	chr18:12421072-12421122	ProgFib	skin:	n/a
46	chr18:12420412-12420462	HNPCEpiC	eye:	n/a
47	chr18:12420862-12420912	HRPEpiC	eye:	n/a
48	chr18:12420862-12420912	SK-N-MC	brain:	n/a
49	chr18:12420862-12420912	GM06990	blood:	n/a
50	chr18:12420862-12420912	GM12891	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12375743..12378274-chr18:12418543..12422031,3	MCF-7	breast:
2	chr18:12418687..12420720-chr18:12430201..12431737,2	MCF-7	breast:
3	chr18:12406749..12409861-chr18:12418820..12421803,8	MCF-7	breast:
4	chr18:12407594..12413164-chr18:12414407..12422412,12	MCF-7	breast:
5	chr18:12418519..12420831-chr18:12657213..12660140,3	MCF-7	breast:
6	chr18:12421209..12423248-chr18:12437108..12438890,2	MCF-7	breast:
7	chr18:12418998..12421842-chr18:12658407..12660489,3	MCF-7	breast:

No data

Variant related genes	Relation type
SLMO1	TF binding region
SLMO1	CpG island
ENSG00000128789	chromatin interactions
ENSG00000141391	chromatin interactions
ENSG00000215527	chromatin interactions
ENSG00000141385	chromatin interactions
ENSG00000134278	chromatin interactions
ENSG00000267199	chromatin interactions
ENSG00000256786	chromatin interactions

Extended variants
information (count: 40 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:40 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372651215	chr18:12420359-12420360	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs139581330	chr18:12420375-12420376	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs150928266	chr18:12420423-12420424	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs535156758	chr18:12420432-12420433	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs566867252	chr18:12420469-12420470	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs199768796	chr18:12420483-12420484	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs372267655	chr18:12420492-12420493	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs375924100	chr18:12420504-12420505	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs567875726	chr18:12420531-12420532	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs538409043	chr18:12420564-12420565	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs529133096	chr18:12420565-12420566	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs547591664	chr18:12420577-12420578	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs538347820	chr18:12420590-12420591	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs553729489	chr18:12420727-12420728	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs369633131	chr18:12420942-12420943	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs12954094	chr18:12420949-12420950	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs571665343	chr18:12420965-12420966	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs542526458	chr18:12420989-12420990	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs554413014	chr18:12421017-12421018	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs59551512	chr18:12421084-12421085	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs543636578	chr18:12421133-12421134	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs28678625	chr18:12421163-12421164	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs533515387	chr18:12421184-12421185	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs545126982	chr18:12421202-12421203	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs560493147	chr18:12421266-12421267	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs527651990	chr18:12421281-12421282	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs549721303	chr18:12421283-12421284	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs146731550	chr18:12421297-12421298	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs551389300	chr18:12421305-12421306	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs566012228	chr18:12421326-12421327	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs140324598	chr18:12421335-12421336	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs550392328	chr18:12421337-12421338	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs571746677	chr18:12421370-12421371	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs538734780	chr18:12421384-12421385	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs547052752	chr18:12421428-12421429	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs565355947	chr18:12421440-12421441	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs3906620	chr18:12421442-12421443	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs112690950	chr18:12421477-12421478	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs576326642	chr18:12421485-12421486	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs371544771	chr18:12421488-12421489	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	4 gene(s)	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	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12410400-12430400	Weak transcription	A549	lung
2	chr18:12418200-12430400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr18:12419600-12420400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr18:12419600-12420600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr18:12419600-12420800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr18:12419600-12421000	Active TSS	Brain Hippocampus Middle	brain
7	chr18:12419600-12421000	Active TSS	Fetal Brain Female	brain
8	chr18:12419800-12420400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr18:12419800-12420400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
10	chr18:12419800-12420400	Flanking Active TSS	Primary hematopoietic stem cells	blood
11	chr18:12419800-12420400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr18:12419800-12420400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr18:12419800-12420400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr18:12419800-12420400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr18:12419800-12420400	Flanking Active TSS	Brain Germinal Matrix	brain
16	chr18:12419800-12420400	Flanking Active TSS	Colonic Mucosa	Colon
17	chr18:12419800-12420400	Active TSS	Fetal Kidney	kidney
18	chr18:12419800-12420400	Flanking Active TSS	Fetal Muscle Trunk	muscle
19	chr18:12419800-12420400	Flanking Active TSS	Placenta	Placenta
20	chr18:12419800-12420400	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
21	chr18:12419800-12420400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr18:12419800-12420600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr18:12419800-12420600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr18:12419800-12420600	Flanking Active TSS	Primary B cells from peripheral blood	blood
25	chr18:12419800-12420600	Active TSS	Primary T cells from cord blood	blood
26	chr18:12419800-12420600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
27	chr18:12419800-12420600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr18:12419800-12420600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr18:12419800-12420600	Active TSS	Colon Smooth Muscle	Colon
30	chr18:12419800-12420600	Active TSS	Duodenum Mucosa	Duodenum
31	chr18:12419800-12420600	Active TSS	Fetal Lung	lung
32	chr18:12419800-12420600	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr18:12419800-12420600	Active TSS	Rectal Mucosa Donor 31	rectum
34	chr18:12419800-12420600	Active TSS	Hela-S3	cervix
35	chr18:12419800-12420600	Active TSS	NHDF-Ad	bronchial
36	chr18:12419800-12420600	Active TSS	NHLF	lung
37	chr18:12419800-12420800	Active TSS	Fetal Intestine Large	intestine
38	chr18:12419800-12420800	Active TSS	Fetal Stomach	stomach
39	chr18:12419800-12420800	Active TSS	Fetal Thymus	thymus
40	chr18:12419800-12420800	Active TSS	Right Ventricle	heart
41	chr18:12419800-12421000	Active TSS	H1 Cell Line	embryonic stem cell
42	chr18:12419800-12421000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr18:12419800-12421000	Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr18:12419800-12421000	Active TSS	Brain Anterior Caudate	brain
45	chr18:12419800-12421000	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr18:12419800-12421000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr18:12419800-12421000	Active TSS	Brain Substantia Nigra	brain
48	chr18:12419800-12421000	Active TSS	Duodenum Smooth Muscle	Duodenum
49	chr18:12419800-12421000	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr18:12419800-12421000	Active TSS	Ovary	ovary

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