Variant report

Variant	nsv983174
Chromosome Location	chr11:18127720-18135636
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	ARID3A	chr11:18127571-18127799	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:18127542-18127787	K562	blood:	n/a	n/a
3	ATF2	chr11:18127440-18127874	GM12878	blood:	n/a	n/a
4	ATF2	chr11:18127600-18127941	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:18127263-18127825	K562	blood:	n/a	n/a
6	BACH1	chr11:18127233-18127848	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr11:18127386-18127944	A549	lung:	n/a	n/a
8	BCL3	chr11:18127334-18127973	A549	lung:	n/a	n/a
9	BCLAF1	chr11:18127404-18127923	GM12878	blood:	n/a	n/a
10	BCLAF1	chr11:18127313-18127906	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:18127532-18127900	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:18127421-18127858	K562	blood:	n/a	n/a
13	BRCA1	chr11:18127349-18127784	GM12878	blood:	n/a	n/a
14	CBX3	chr11:18127389-18127961	K562	blood:	n/a	n/a
15	CBX3	chr11:18127290-18127881	HCT-116	colon:	n/a	n/a
16	CCNT2	chr11:18127203-18127809	K562	blood:	n/a	chr11:18127745-18127754
17	CEBPB	chr11:18127442-18127781	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:18127585-18127843	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPD	chr11:18127454-18127787	HepG2	liver:	n/a	n/a
20	CHD1	chr11:18127518-18127870	GM12878	blood:	n/a	n/a
21	CHD2	chr11:18127394-18127847	HepG2	liver:	n/a	n/a
22	CHD2	chr11:18127409-18127914	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr11:18127425-18127833	K562	blood:	n/a	n/a
24	CHD2	chr11:18127337-18127907	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr11:18127354-18127912	GM12878	blood:	n/a	n/a
26	CREB1	chr11:18127252-18127961	HepG2	liver:	n/a	n/a
27	CREB1	chr11:18127392-18127795	A549	lung:	n/a	n/a
28	CTCF	chr11:18127640-18127790	AG09309	skin:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
29	CTCF	chr11:18127600-18127750	WERI-Rb-1	eye:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
30	CTCF	chr11:18134560-18134710	HEK293	kidney:	n/a	n/a
31	CTCF	chr11:18128200-18128350	GM12873	blood:	n/a	n/a
32	CTCF	chr11:18127600-18127750	SAEC	small airway:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
33	CTCF	chr11:18127560-18127860	GM13976	blood:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
34	CTCF	chr11:18128140-18128290	AG09319	gingival:	n/a	n/a
35	CTCF	chr11:18127660-18127810	SAEC	small airway:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
36	CTCF	chr11:18127920-18128012	GM10248	blood:	n/a	n/a
37	CTCF	chr11:18127532-18127825	SK-N-SH_RA	brain:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
38	CTCF	chr11:18127640-18127790	HCFaa	heart:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
39	CTCF	chr11:18127480-18127883	GM12892	blood:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
40	CTCF	chr11:18127640-18127790	GM12870	blood:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
41	CTCF	chr11:18127600-18127750	HepG2	liver:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
42	CTCF	chr11:18127640-18127790	GM12873	blood:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
43	CTCF	chr11:18127593-18127834	GM10248	blood:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
44	CTCF	chr11:18127528-18127873	GM12878	blood:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
45	CTCF	chr11:18127927-18127979	GM19239	blood:	n/a	n/a
46	CTCF	chr11:18127970-18127992	GM19238	blood:	n/a	n/a
47	CTCF	chr11:18127640-18127790	HVMF	connective:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
48	CTCF	chr11:18127423-18127918	GM12878	blood:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711
49	CTCF	chr11:18127907-18127977	Fibrobl	skin:	n/a	n/a
50	CTCF	chr11:18127620-18127770	GM06990	blood:	n/a	chr11:18127688-18127709 chr11:18127694-18127710 chr11:18127693-18127711

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18127676-18127726	AoSMC	blood vessel:	n/a
2	chr11:18128126-18128176	AG10803	skin:	n/a
3	chr11:18127958-18128008	NHBE	bronchial:	n/a
4	chr11:18130049-18130099	LNCaP	prostate:	n/a
5	chr11:18130049-18130099	GM12891	blood:	n/a
6	chr11:18127696-18127746	AG09319	gingival:	n/a
7	chr11:18127676-18127726	SAEC	small airway:	n/a
8	chr11:18127958-18128008	K562	blood:	n/a
9	chr11:18128126-18128176	CMK	blood:	n/a
10	chr11:18128177-18128227	AoSMC	blood vessel:	n/a
11	chr11:18127676-18127726	BE2_C	brain:	n/a
12	chr11:18127696-18127746	IMR90	lung:	fetal
13	chr11:18127958-18128008	MCF10A-Er-Src	breast:	n/a
14	chr11:18130049-18130099	RPTEC	kidney:	n/a
15	chr11:18128177-18128227	SK-N-MC	brain:	n/a
16	chr11:18127696-18127746	AG10803	skin:	n/a
17	chr11:18127696-18127746	NB4	blood:	n/a
18	chr11:18127958-18128008	H1-hESC	embryonic stem cell:	embryo
19	chr11:18128126-18128176	NB4	blood:	n/a
20	chr11:18127696-18127746	HMEC	breast:	n/a
21	chr11:18127696-18127746	ovcar-3	ovarian:	n/a
22	chr11:18128177-18128227	HCF	heart:	n/a
23	chr11:18127696-18127746	CMK	blood:	n/a
24	chr11:18130049-18130099	AG04449	skin:	fetal
25	chr11:18127676-18127726	PFSK-1	brain:	n/a
26	chr11:18127676-18127726	ovcar-3	ovarian:	n/a
27	chr11:18127696-18127746	BJ	skin:	n/a
28	chr11:18127676-18127726	PANC-1	pancreas:	n/a
29	chr11:18127958-18128008	IMR90	lung:	fetal
30	chr11:18127958-18128008	PANC-1	pancreas:	n/a
31	chr11:18130049-18130099	Caco-2	colon:	n/a
32	chr11:18128177-18128227	AG10803	skin:	n/a
33	chr11:18128126-18128176	AG09319	gingival:	n/a
34	chr11:18127696-18127746	GM06990	blood:	n/a
35	chr11:18127696-18127746	HRCEpiC	kidney:	n/a
36	chr11:18127696-18127746	SKMC	muscle:	n/a
37	chr11:18130049-18130099	HCF	heart:	n/a
38	chr11:18127958-18128008	HIPEpiC	eye:	n/a
39	chr11:18130049-18130099	HNPCEpiC	eye:	n/a
40	chr11:18128177-18128227	PrEC	prostate:	n/a
41	chr11:18128177-18128227	GM12878	blood:	n/a
42	chr11:18128177-18128227	MCF-7	breast:	n/a
43	chr11:18130049-18130099	NH-A	brain:	n/a
44	chr11:18127676-18127726	HCF	heart:	n/a
45	chr11:18127696-18127746	LNCaP	prostate:	n/a
46	chr11:18128177-18128227	HEEpiC	esophagus:	n/a
47	chr11:18128177-18128227	NHDF-neo	bronchial:	n/a
48	chr11:18128177-18128227	U87	brain:	n/a
49	chr11:18130049-18130099	NHDF-neo	bronchial:	n/a
50	chr11:18127958-18128008	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:18127425..18129160-chr11:18131186..18134005,2	K562	blood:
2	chr11:18034152..18035903-chr11:18125561..18127722,2	MCF-7	breast:
3	chr11:18126132..18128998-chr11:18342491..18344042,2	K562	blood:
4	chr11:18126284..18129283-chr11:18131748..18134155,2	MCF-7	breast:
5	chr11:18129937..18132651-chr11:18134696..18136776,2	K562	blood:
6	chr11:18126382..18129107-chr11:18133072..18137043,3	K562	blood:
7	chr11:18013230..18013986-chr11:18128436..18129004,2	K562	blood:
8	chr11:18127813..18129704-chr11:18132891..18135867,2	MCF-7	breast:
9	chr11:18129937..18132651-chr11:18134696..18136776,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRGPRX3-1	chr11:18128130-18128388	NONHSAT018261
2	lnc-SAAL1-1	chr11:18134699-18134839	NONHSAT018263
3	lnc-SAAL1-1	chr11:18134173-18134308	NONHSAT018263

Variant related genes	Relation type
SAAL1	TF binding region
HIGD1AP5	TF binding region
SAAL1	CpG island
HIGD1AP5	CpG island
ENSG00000110756	chromatin interactions
ENSG00000166788	chromatin interactions
ENSG00000110768	chromatin interactions
ENSG00000255254	chromatin interactions
ENSG00000129158	chromatin interactions

Extended variants
information (count: 313 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:313 , 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	rs189119994	chr11:18127720-18127721	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs564522865	chr11:18127721-18127722	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs531885971	chr11:18127739-18127740	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs549991581	chr11:18127751-18127752	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs564255834	chr11:18127758-18127759	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs138925854	chr11:18127762-18127763	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs192471973	chr11:18127782-18127783	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs547640418	chr11:18127786-18127787	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs565846485	chr11:18127835-18127836	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs149440092	chr11:18127907-18127908	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs557379106	chr11:18127910-18127911	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs376745788	chr11:18127911-18127912	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs575724540	chr11:18127918-18127919	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs536786573	chr11:18127919-18127920	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs16934941	chr11:18127921-18127922	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs574951883	chr11:18127958-18127959	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs531547502	chr11:18127965-18127966	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs146357795	chr11:18127977-18127978	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs12291516	chr11:18128018-18128019	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs184655941	chr11:18128043-18128044	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs557220170	chr11:18128047-18128048	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs74972390	chr11:18128172-18128173	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs531822878	chr11:18128182-18128183	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs543993880	chr11:18128208-18128209	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs543960853	chr11:18128242-18128243	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs187515185	chr11:18128247-18128248	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs529049602	chr11:18128318-18128319	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs547278276	chr11:18128357-18128358	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs12292912	chr11:18128364-18128365	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs139729754	chr11:18128365-18128366	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs141626561	chr11:18128383-18128384	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs548249687	chr11:18128392-18128393	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs569340415	chr11:18128443-18128444	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs146201294	chr11:18128465-18128466	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs555013323	chr11:18128529-18128530	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs148430108	chr11:18128578-18128579	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs535994740	chr11:18128603-18128604	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs12293054	chr11:18128644-18128645	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546552461	chr11:18128656-18128657	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs374127357	chr11:18128697-18128698	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs374911615	chr11:18128707-18128708	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs576477825	chr11:18128754-18128755	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs7129230	chr11:18128755-18128756	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536954574	chr11:18128804-18128805	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs7129345	chr11:18128825-18128826	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs11024493	chr11:18128834-18128835	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs541211483	chr11:18128841-18128842	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559319728	chr11:18128846-18128847	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs533038688	chr11:18128854-18128855	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551236002	chr11:18128894-18128895	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD

Chromatin state (count:229 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18125800-18128000	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr11:18126000-18127800	Active TSS	Muscle Satellite Cultured Cells	--
3	chr11:18126000-18128000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:18126000-18128200	Active TSS	A549	lung
5	chr11:18126200-18127800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:18126200-18128000	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr11:18126200-18128000	Active TSS	H9 Cell Line	embryonic stem cell
8	chr11:18126200-18128000	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr11:18126200-18128000	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr11:18126400-18127800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:18126400-18127800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr11:18126400-18127800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:18126400-18127800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr11:18126400-18128000	Active TSS	H1 Cell Line	embryonic stem cell
15	chr11:18126400-18128000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:18126400-18128000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:18126400-18128000	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr11:18126400-18128000	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr11:18126400-18128000	Active TSS	NH-A	brain
20	chr11:18126400-18128200	Active TSS	Ovary	ovary
21	chr11:18126400-18128200	Active TSS	NHDF-Ad	bronchial
22	chr11:18126600-18127800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr11:18126600-18127800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:18126600-18127800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:18126600-18127800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:18126600-18127800	Active TSS	Fetal Kidney	kidney
27	chr11:18126600-18127800	Active TSS	Rectal Smooth Muscle	rectum
28	chr11:18126600-18127800	Active TSS	Right Ventricle	heart
29	chr11:18126600-18128000	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr11:18126600-18128000	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr11:18126600-18128000	Active TSS	Brain Substantia Nigra	brain
32	chr11:18126600-18128000	Active TSS	GM12878-XiMat	blood
33	chr11:18126600-18128000	Active TSS	HSMM	muscle
34	chr11:18126600-18128000	Active TSS	K562	blood
35	chr11:18126600-18128000	Active TSS	NHLF	lung
36	chr11:18126600-18128200	Active TSS	Brain Angular Gyrus	brain
37	chr11:18126600-18128200	Active TSS	Fetal Brain Female	brain
38	chr11:18126600-18128200	Active TSS	Psoas Muscle	Psoas
39	chr11:18126600-18128400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:18126600-18128400	Active TSS	Fetal Brain Male	brain
41	chr11:18126800-18127800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:18126800-18127800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:18126800-18127800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr11:18126800-18127800	Active TSS	Esophagus	oesophagus
45	chr11:18126800-18127800	Active TSS	Fetal Intestine Large	intestine
46	chr11:18126800-18127800	Active TSS	Fetal Intestine Small	intestine
47	chr11:18126800-18127800	Active TSS	HUVEC	blood vessel
48	chr11:18126800-18128000	Active TSS	Brain Germinal Matrix	brain
49	chr11:18126800-18128000	Active TSS	Colonic Mucosa	Colon
50	chr11:18126800-18128000	Active TSS	Rectal Mucosa Donor 29	rectum

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