Variant report

Variant	esv3356225
Chromosome Location	chr11:67414976-67419374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:431)
CpG islands
(count:793)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:67416556-67417488	GM12878	blood:	n/a	n/a
2	BCL11A	chr11:67416654-67417245	GM12878	blood:	n/a	chr11:67416891-67416900
3	BCL3	chr11:67416629-67417679	GM12878	blood:	n/a	chr11:67416891-67416900
4	BCL3	chr11:67416602-67417626	GM12878	blood:	n/a	chr11:67416891-67416900
5	BCLAF1	chr11:67417791-67418254	GM12878	blood:	n/a	chr11:67418101-67418115
6	BCLAF1	chr11:67416501-67417143	GM12878	blood:	n/a	chr11:67416891-67416900
7	BHLHE40	chr11:67415669-67415776	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:67416730-67417113	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:67417215-67417294	K562	blood:	n/a	n/a
10	BRCA1	chr11:67417041-67417787	GM12878	blood:	n/a	n/a
11	CBX3	chr11:67417207-67417601	K562	blood:	n/a	n/a
12	CEBPB	chr11:67415694-67415820	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr11:67416678-67417514	GM12878	blood:	n/a	n/a
14	CHD2	chr11:67416690-67417392	GM12878	blood:	n/a	n/a
15	CHD2	chr11:67415717-67415894	GM12878	blood:	n/a	n/a
16	CTCF	chr11:67415740-67415890	HEK293	kidney:	n/a	n/a
17	CTCF	chr11:67415660-67415810	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr11:67415709-67415832	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr11:67415680-67415830	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr11:67415680-67415830	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr11:67415740-67415890	GM12866	blood:	n/a	n/a
22	CTCF	chr11:67415576-67415942	HepG2	liver:	n/a	n/a
23	CTCF	chr11:67415660-67415810	HCT-116	colon:	n/a	n/a
24	CTCF	chr11:67415659-67415876	GM10266	blood:	n/a	n/a
25	CTCF	chr11:67415700-67415850	K562	blood:	n/a	n/a
26	CTCF	chr11:67415542-67415960	K562	blood:	n/a	chr11:67415945-67415958
27	CTCF	chr11:67415700-67415855	Fibrobl	skin:	n/a	n/a
28	CTCF	chr11:67415634-67415920	MCF-7	breast:	n/a	n/a
29	CTCF	chr11:67415700-67415850	A549	lung:	n/a	n/a
30	CTCF	chr11:67415060-67415210	GM12867	blood:	n/a	n/a
31	CTCF	chr11:67415720-67415870	GM12868	blood:	n/a	n/a
32	CTCF	chr11:67415680-67415830	RPTEC	kidney:	n/a	n/a
33	CTCF	chr11:67417040-67417190	GM12873	blood:	n/a	n/a
34	CTCF	chr11:67417200-67417350	GM12873	blood:	n/a	n/a
35	CTCF	chr11:67415680-67415830	BJ	skin:	n/a	n/a
36	CTCF	chr11:67415680-67415830	GM12865	blood:	n/a	n/a
37	CTCF	chr11:67415680-67415830	HMEC	breast:	n/a	n/a
38	CTCF	chr11:67415724-67415866	Lung_OC	lung:	n/a	n/a
39	CTCF	chr11:67415720-67415870	GM12878	blood:	n/a	n/a
40	CTCF	chr11:67415680-67415830	AG10803	skin:	n/a	n/a
41	CTCF	chr11:67415700-67415850	HepG2	liver:	n/a	n/a
42	CTCF	chr11:67416340-67416490	GM06990	blood:	n/a	chr11:67416399-67416412 chr11:67416399-67416408 chr11:67416393-67416406
43	CTCF	chr11:67417000-67417150	GM12873	blood:	n/a	n/a
44	CTCF	chr11:67417013-67417460	GM12892	blood:	n/a	n/a
45	CTCF	chr11:67415670-67415871	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr11:67415578-67415954	A549	lung:	n/a	n/a
47	CTCF	chr11:67415638-67415906	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr11:67415451-67416092	MCF-7	breast:	n/a	chr11:67415945-67415958
49	CTCF	chr11:67415422-67416058	HCT-116	colon:	n/a	chr11:67415945-67415958
50	CTCF	chr11:67415600-67415750	AG04450	lung:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67418213-67418263	BJ	skin:	n/a
2	chr11:67418113-67418163	ECC-1	luminal epithelium:	n/a
3	chr11:67418045-67418095	SKMC	muscle:	n/a
4	chr11:67418045-67418095	GM12891	blood:	n/a
5	chr11:67418148-67418198	PANC-1	pancreas:	n/a
6	chr11:67418106-67418156	HCPEpiC	choroid plexus:	n/a
7	chr11:67418213-67418263	NB4	blood:	n/a
8	chr11:67418365-67418415	HCT-116	colon:	n/a
9	chr11:67418113-67418163	BE2_C	brain:	n/a
10	chr11:67418113-67418163	BJ	skin:	n/a
11	chr11:67418140-67418190	SK-N-MC	brain:	n/a
12	chr11:67418213-67418263	AG04450	lung:	fetal
13	chr11:67418358-67418408	Caco-2	colon:	n/a
14	chr11:67418365-67418415	MCF10A-Er-Src	breast:	n/a
15	chr11:67418140-67418190	HIPEpiC	eye:	n/a
16	chr11:67418365-67418415	SK-N-SH_RA	brain:	n/a
17	chr11:67418358-67418408	AoSMC	blood vessel:	n/a
18	chr11:67418213-67418263	HMEC	breast:	n/a
19	chr11:67418405-67418455	U87	brain:	n/a
20	chr11:67418140-67418190	ovcar-3	ovarian:	n/a
21	chr11:67418405-67418455	PANC-1	pancreas:	n/a
22	chr11:67418148-67418198	CMK	blood:	n/a
23	chr11:67418365-67418415	HRCEpiC	kidney:	n/a
24	chr11:67417958-67418008	SK-N-SH	brain:	n/a
25	chr11:67418405-67418455	GM12892	blood:	n/a
26	chr11:67417958-67418008	HL-60	blood:	n/a
27	chr11:67418358-67418408	LNCaP	prostate:	n/a
28	chr11:67418405-67418455	HRE	kidney:	n/a
29	chr11:67418405-67418455	LNCaP	prostate:	n/a
30	chr11:67418310-67418360	U87	brain:	n/a
31	chr11:67418148-67418198	AG10803	skin:	n/a
32	chr11:67418358-67418408	NT2-D1	testis:	n/a
33	chr11:67418310-67418360	ProgFib	skin:	n/a
34	chr11:67418213-67418263	Hepatocyte	liver:	n/a
35	chr11:67418358-67418408	GM12892	blood:	n/a
36	chr11:67418315-67418365	GM12891	blood:	n/a
37	chr11:67418358-67418408	HCF	heart:	n/a
38	chr11:67418106-67418156	AoSMC	blood vessel:	n/a
39	chr11:67418291-67418341	HRCEpiC	kidney:	n/a
40	chr11:67418213-67418263	NH-A	brain:	n/a
41	chr11:67418291-67418341	HRPEpiC	eye:	n/a
42	chr11:67418045-67418095	A549	lung:	n/a
43	chr11:67418405-67418455	GM12891	blood:	n/a
44	chr11:67418291-67418341	BE2_C	brain:	n/a
45	chr11:67418291-67418341	NHDF-neo	bronchial:	n/a
46	chr11:67418405-67418455	HepG2	liver:	n/a
47	chr11:67418310-67418360	ECC-1	luminal epithelium:	n/a
48	chr11:67418045-67418095	RPTEC	kidney:	n/a
49	chr11:67418405-67418455	NH-A	brain:	n/a
50	chr11:67418213-67418263	PrEC	prostate:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67412966..67415782-chr11:67417103..67418705,2	K562	blood:
2	chr11:67397789..67398746-chr11:67415579..67416141,2	MCF-7	breast:
3	chr11:67415991..67416960-chr11:67457830..67458791,2	MCF-7	breast:
4	chr11:67340062..67340769-chr11:67415307..67416088,2	MCF-7	breast:
5	chr11:67415337..67416268-chr11:67458366..67459257,5	MCF-7	breast:
6	chr11:67396434..67397233-chr11:67415377..67416192,2	MCF-7	breast:
7	chr11:67412966..67415782-chr11:67417103..67418705,2	K562	blood:
8	chr11:67415666..67416189-chr11:67426687..67427517,2	MCF-7	breast:
9	chr11:67275644..67277559-chr11:67415737..67417580,2	K562	blood:
10	chr11:67415318..67416230-chr11:67426559..67427542,5	MCF-7	breast:
11	chr11:67404297..67409206-chr11:67410255..67415069,8	MCF-7	breast:
12	chr11:67395494..67399201-chr11:67413492..67416311,3	K562	blood:
13	chr11:67396543..67400484-chr11:67414425..67419634,5	MCF-7	breast:
14	chr11:67141089..67142722-chr11:67418799..67420711,2	K562	blood:

No data

Variant related genes	Relation type
ACY3	TF binding region
ACY3	CpG island
ENSG00000167799	chromatin interactions
ENSG00000132744	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000167800	chromatin interactions

Extended variants
information (count: 267 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368214614	chr11:67414979-67414980	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs371939667	chr11:67414987-67414988	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs182253588	chr11:67414988-67414989	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs556225865	chr11:67414992-67414993	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs536560394	chr11:67414996-67414997	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs574733600	chr11:67415008-67415009	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs187282641	chr11:67415026-67415027	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs554169358	chr11:67415027-67415028	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs572656219	chr11:67415028-67415029	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs539863221	chr11:67415037-67415038	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs2514036	chr11:67415054-67415055	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs577198990	chr11:67415108-67415109	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs2509716	chr11:67415136-67415137	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs540883989	chr11:67415150-67415151	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs115777389	chr11:67415163-67415164	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs529918934	chr11:67415183-67415184	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs548325060	chr11:67415188-67415189	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs566669406	chr11:67415208-67415209	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554408635	chr11:67415212-67415213	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs141339224	chr11:67415214-67415215	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs373948069	chr11:67415215-67415216	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574047086	chr11:67415238-67415239	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs116235786	chr11:67415279-67415280	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs554010265	chr11:67415288-67415289	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs190826884	chr11:67415318-67415319	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs183012360	chr11:67415319-67415320	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs115596420	chr11:67415376-67415377	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs150304467	chr11:67415378-67415379	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs535660572	chr11:67415400-67415401	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs185709299	chr11:67415424-67415425	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs375824915	chr11:67415431-67415432	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs76605945	chr11:67415463-67415464	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs540154851	chr11:67415473-67415474	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs137875827	chr11:67415510-67415511	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs576952877	chr11:67415556-67415557	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs544291981	chr11:67415613-67415614	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs143539665	chr11:67415699-67415700	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs147155441	chr11:67415714-67415715	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs556025276	chr11:67415717-67415718	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs61894520	chr11:67415753-67415754	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs373086207	chr11:67415789-67415790	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs190128580	chr11:67415806-67415807	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs77761047	chr11:67415827-67415828	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs112459428	chr11:67415829-67415830	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs369274588	chr11:67415835-67415836	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs75228064	chr11:67415890-67415891	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs571971725	chr11:67415926-67415927	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs552487436	chr11:67415929-67415930	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs564039060	chr11:67415938-67415939	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs117523325	chr11:67415955-67415956	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67398800-67418600	Weak transcription	Right Atrium	heart
2	chr11:67408000-67417000	Weak transcription	Gastric	stomach
3	chr11:67408200-67416400	Weak transcription	Stomach Mucosa	stomach
4	chr11:67409800-67417000	Weak transcription	HepG2	liver
5	chr11:67410400-67417000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr11:67410400-67417000	Weak transcription	Liver	Liver
7	chr11:67411600-67417000	Weak transcription	Brain Hippocampus Middle	brain
8	chr11:67411800-67416000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr11:67411800-67417200	Enhancers	Primary B cells from peripheral blood	blood
10	chr11:67411800-67417600	Enhancers	Pancreas	Pancrea
11	chr11:67411800-67419600	Enhancers	Primary B cells from cord blood	blood
12	chr11:67412200-67420600	Enhancers	Primary hematopoietic stem cells	blood
13	chr11:67412400-67416800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr11:67412400-67417800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:67412600-67417600	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr11:67412800-67418000	Enhancers	Spleen	Spleen
17	chr11:67413000-67417000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr11:67413000-67417600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:67413200-67417000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:67413400-67415000	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr11:67413400-67417800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr11:67413600-67415200	Flanking Active TSS	Duodenum Mucosa	Duodenum
23	chr11:67413600-67415200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr11:67413600-67415600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr11:67413600-67415800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr11:67413600-67416400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr11:67413600-67417400	Genic enhancers	Fetal Intestine Small	intestine
28	chr11:67413600-67417800	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr11:67413600-67417800	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr11:67413600-67418000	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr11:67413800-67415000	Enhancers	Small Intestine	intestine
32	chr11:67413800-67418000	Enhancers	Thymus	Thymus
33	chr11:67414000-67417000	Weak transcription	Brain Substantia Nigra	brain
34	chr11:67414200-67416400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
35	chr11:67414200-67416600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
36	chr11:67414400-67415000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
37	chr11:67414400-67415800	Weak transcription	Rectal Smooth Muscle	rectum
38	chr11:67414400-67417800	Enhancers	Placenta	Placenta
39	chr11:67414600-67415000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr11:67414600-67415400	Enhancers	Colonic Mucosa	Colon
41	chr11:67414600-67415800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:67414600-67415800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr11:67414600-67416200	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr11:67414600-67416400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr11:67414600-67417000	Weak transcription	Esophagus	oesophagus
46	chr11:67414600-67417400	Enhancers	Fetal Intestine Large	intestine
47	chr11:67414600-67417800	Enhancers	Primary T cells fromperipheralblood	blood
48	chr11:67414600-67417800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr11:67414600-67418000	Enhancers	Fetal Thymus	thymus
50	chr11:67414800-67416600	Weak transcription	Primary T cells from cord blood	blood

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