Variant report

Variant	esv3448805
Chromosome Location	chr11:65099726-65102224
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	ATF3	chr11:65100961-65101550	A549	lung:	n/a	chr11:65101240-65101249
2	ATF3	chr11:65101065-65101549	A549	lung:	n/a	chr11:65101240-65101249
3	BACH1	chr11:65101075-65101549	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr11:65101050-65101715	GM12878	blood:	n/a	n/a
5	BRCA1	chr11:65101181-65101629	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr11:65101537-65101701	GM12878	blood:	n/a	n/a
7	CBX3	chr11:65100971-65101701	K562	blood:	n/a	n/a
8	CCNT2	chr11:65101100-65101805	K562	blood:	n/a	n/a
9	CEBPB	chr11:65101409-65101565	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:65101184-65101407	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:65101148-65101576	Hela-S3	cervix:	n/a	chr11:65101557-65101569
12	CEBPD	chr11:65101115-65101514	HepG2	liver:	n/a	n/a
13	CHD1	chr11:65100985-65103307	IMR90	lung:	n/a	chr11:65101777-65101787
14	CHD1	chr11:65101303-65101834	H1-hESC	embryonic stem cell:	n/a	chr11:65101777-65101787
15	CHD1	chr11:65101286-65101710	GM12878	blood:	n/a	n/a
16	CHD2	chr11:65101134-65101860	Hela-S3	cervix:	n/a	chr11:65101777-65101787
17	CHD2	chr11:65101228-65101619	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr11:65101665-65101695	K562	blood:	n/a	n/a
19	CHD2	chr11:65101496-65101696	HepG2	liver:	n/a	n/a
20	CHD2	chr11:65101144-65101524	GM12878	blood:	n/a	n/a
21	CREB1	chr11:65100967-65101777	A549	lung:	n/a	n/a
22	CTCF	chr11:65101520-65101670	GM12868	blood:	n/a	chr11:65101578-65101591 chr11:65101576-65101585
23	CTCF	chr11:65101420-65101570	Hela-S3	cervix:	n/a	chr11:65101504-65101522 chr11:65101510-65101519
24	CTCF	chr11:65101440-65101590	Hela-S3	cervix:	n/a	chr11:65101504-65101522 chr11:65101576-65101585 chr11:65101510-65101519
25	CTCF	chr11:65101420-65101570	K562	blood:	n/a	chr11:65101504-65101522 chr11:65101510-65101519
26	CTCF	chr11:65101500-65101650	AG04450	lung:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
27	CTCF	chr11:65101480-65101630	HAc	cerebellar:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
28	CTCF	chr11:65101223-65101364	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr11:65101480-65101630	SK-N-SH_RA	brain:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
30	CTCF	chr11:65101480-65101630	HMEC	breast:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
31	CTCF	chr11:65101440-65101590	HPAF	blood vessel:	n/a	chr11:65101504-65101522 chr11:65101576-65101585 chr11:65101510-65101519
32	CTCF	chr11:65101460-65101610	HVMF	connective:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
33	CTCF	chr11:65101500-65101650	HRPEpiC	eye:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
34	CTCF	chr11:65101576-65101591	A549	lung:	n/a	chr11:65101578-65101591 chr11:65101576-65101585
35	CTCF	chr11:65101424-65101722	K562	blood:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
36	CTCF	chr11:65101488-65101548	Pancreas_OC	pancreas:	n/a	chr11:65101504-65101522 chr11:65101510-65101519
37	CTCF	chr11:65101400-65101550	HBMEC	blood vessel:	n/a	chr11:65101504-65101522 chr11:65101510-65101519
38	CTCF	chr11:65101300-65101450	HAc	cerebellar:	n/a	n/a
39	CTCF	chr11:65101460-65101610	AG04449	skin:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
40	CTCF	chr11:65101460-65101610	HUVEC	blood vessel:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
41	CTCF	chr11:65101460-65101610	BJ	skin:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
42	CTCF	chr11:65101480-65101630	GM12875	blood:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
43	CTCF	chr11:65101549-65101632	GM19240	blood:	n/a	chr11:65101578-65101591 chr11:65101576-65101585
44	CTCF	chr11:65101500-65101650	GM12871	blood:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
45	CTCF	chr11:65101500-65101650	AG04449	skin:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
46	CTCF	chr11:65101540-65101690	GM12871	blood:	n/a	chr11:65101578-65101591 chr11:65101576-65101585
47	CTCF	chr11:65101420-65101570	AG10803	skin:	n/a	chr11:65101504-65101522 chr11:65101510-65101519
48	CTCF	chr11:65101405-65101605	IMR90	lung:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
49	CTCF	chr11:65101398-65101622	K562	blood:	n/a	chr11:65101504-65101522 chr11:65101578-65101591 chr11:65101576-65101585 chr11:65101510-65101519
50	CTCF	chr11:65101440-65101590	MCF-7	breast:	n/a	chr11:65101504-65101522 chr11:65101576-65101585 chr11:65101510-65101519

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65101065-65101115	MCF-7	breast:	n/a
2	chr11:65101065-65101115	MCF-7	breast:	n/a
3	chr11:65101842-65101892	PFSK-1	brain:	n/a
4	chr11:65101167-65101217	A549	lung:	n/a
5	chr11:65101167-65101217	GM19239	blood:	n/a
6	chr11:65101602-65101652	RPTEC	kidney:	n/a
7	chr11:65101602-65101652	U87	brain:	n/a
8	chr11:65101602-65101652	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:65101065-65101115	SK-N-SH_RA	brain:	n/a
10	chr11:65101156-65101206	LNCaP	prostate:	n/a
11	chr11:65101602-65101652	AG04449	skin:	fetal
12	chr11:65101602-65101652	AG09309	skin:	n/a
13	chr11:65101167-65101217	AG09319	gingival:	n/a
14	chr11:65101539-65101589	AG04449	skin:	fetal
15	chr11:65101167-65101217	U87	brain:	n/a
16	chr11:65101156-65101206	AG10803	skin:	n/a
17	chr11:65101602-65101652	BE2_C	brain:	n/a
18	chr11:65101065-65101115	GM19239	blood:	n/a
19	chr11:65101075-65101125	RPTEC	kidney:	n/a
20	chr11:65101075-65101125	SK-N-SH	brain:	n/a
21	chr11:65101602-65101652	PrEC	prostate:	n/a
22	chr11:65101602-65101652	Hela-S3	cervix:	n/a
23	chr11:65101842-65101892	NHDF-neo	bronchial:	n/a
24	chr11:65101156-65101206	T-47D	breast:	n/a
25	chr11:65101156-65101206	HEEpiC	esophagus:	n/a
26	chr11:65101065-65101115	Hepatocyte	liver:	n/a
27	chr11:65101842-65101892	U87	brain:	n/a
28	chr11:65101539-65101589	PFSK-1	brain:	n/a
29	chr11:65101842-65101892	SKMC	muscle:	n/a
30	chr11:65101167-65101217	Jurkat	blood:	n/a
31	chr11:65101539-65101589	GM06990	blood:	n/a
32	chr11:65101156-65101206	HRCEpiC	kidney:	n/a
33	chr11:65101602-65101652	HepG2	liver:	n/a
34	chr11:65101842-65101892	HRCEpiC	kidney:	n/a
35	chr11:65101539-65101589	CMK	blood:	n/a
36	chr11:65101065-65101115	IMR90	lung:	fetal
37	chr11:65101602-65101652	Jurkat	blood:	n/a
38	chr11:65101842-65101892	A549	lung:	n/a
39	chr11:65101167-65101217	NHBE	bronchial:	n/a
40	chr11:65101065-65101115	PrEC	prostate:	n/a
41	chr11:65101156-65101206	SKMC	muscle:	n/a
42	chr11:65101156-65101206	Jurkat	blood:	n/a
43	chr11:65101842-65101892	HNPCEpiC	eye:	n/a
44	chr11:65101065-65101115	Jurkat	blood:	n/a
45	chr11:65101842-65101892	Hepatocyte	liver:	n/a
46	chr11:65101156-65101206	SK-N-SH	brain:	n/a
47	chr11:65101156-65101206	GM19239	blood:	n/a
48	chr11:65101602-65101652	HAEpiC	amniotic membrane:	n/a
49	chr11:65101156-65101206	HCF	heart:	n/a
50	chr11:65101842-65101892	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65081241..65085742-chr11:65099388..65103053,6	MCF-7	breast:
2	chr11:65100087..65102594-chr11:65381500..65383141,2	MCF-7	breast:
3	chr11:65099718..65102956-chr11:65121267..65125924,4	MCF-7	breast:
4	chr11:65082396..65084824-chr11:65098924..65101432,3	MCF-7	breast:
5	chr11:65077010..65079617-chr11:65101633..65103467,2	K562	blood:
6	chr11:65029300..65032261-chr11:65099980..65102412,3	K562	blood:
7	chr11:64862541..64864167-chr11:65101190..65102852,2	MCF-7	breast:
8	chr11:65099880..65103900-chr11:65265146..65267934,3	MCF-7	breast:
9	chr11:65099781..65103974-chr11:65120675..65126515,7	MCF-7	breast:
10	chr11:65096087..65101158-chr11:65187507..65191685,6	K562	blood:
11	chr11:65101009..65102671-chr11:65109957..65112213,2	K562	blood:
12	chr11:65101528..65104353-chr11:65197990..65200376,2	K562	blood:
13	chr11:65100032..65102632-chr11:65307572..65309259,3	MCF-7	breast:
14	chr11:65100322..65103953-chr11:65104304..65109119,7	MCF-7	breast:
15	chr11:65102149..65103973-chr11:65118677..65120435,2	MCF-7	breast:
16	chr11:65100635..65103447-chr11:65112370..65113916,2	K562	blood:
17	chr11:65101646..65104320-chr11:65195923..65197643,2	K562	blood:
18	chr11:65098368..65100448-chr11:65187507..65189022,2	K562	blood:
19	chr11:65097328..65098970-chr11:65099597..65101116,2	MCF-7	breast:
20	chr11:65100243..65104610-chr11:65105410..65109851,8	K562	blood:
21	chr11:65098911..65102850-chr11:65147012..65151675,4	MCF-7	breast:
22	chr11:65081631..65084592-chr11:65099872..65104597,5	K562	blood:
23	chr11:65028467..65031251-chr11:65099786..65102995,3	MCF-7	breast:
24	chr11:65082224..65084911-chr11:65099875..65102878,3	K562	blood:

Variant related genes	Relation type
DPF2	TF binding region
DPF2	CpG island
ENSG00000149823	chromatin interactions
ENSG00000173327	chromatin interactions
ENSG00000168056	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000162241	chromatin interactions
ENSG00000173825	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000014138	chromatin interactions
ENSG00000149798	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000133884	chromatin interactions

Extended variants
information (count: 144 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:144 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370101833	chr11:65099745-65099746	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs112857572	chr11:65099757-65099758	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs12274694	chr11:65099777-65099778	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs555485606	chr11:65099861-65099862	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs116742819	chr11:65099893-65099894	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs535459170	chr11:65099902-65099903	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs555767426	chr11:65099928-65099929	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs113033312	chr11:65099948-65099949	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs184006657	chr11:65099980-65099981	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs113815291	chr11:65099990-65099991	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs535227098	chr11:65100007-65100008	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs556075614	chr11:65100014-65100015	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs563890883	chr11:65100065-65100066	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs188694969	chr11:65100068-65100069	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs540075024	chr11:65100075-65100076	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs560181649	chr11:65100105-65100106	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs529212209	chr11:65100116-65100117	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs548670320	chr11:65100124-65100125	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs562527406	chr11:65100126-65100127	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs28781278	chr11:65100137-65100138	Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551512170	chr11:65100157-65100158	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs146942767	chr11:65100164-65100165	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs180887245	chr11:65100192-65100193	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs113927625	chr11:65100207-65100208	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs117966430	chr11:65100224-65100225	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs536161241	chr11:65100251-65100252	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs563030631	chr11:65100359-65100360	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs555447699	chr11:65100362-65100363	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs575235353	chr11:65100387-65100388	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs544643894	chr11:65100449-65100450	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs35018170	chr11:65100451-65100452	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs140362866	chr11:65100452-65100453	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs564941400	chr11:65100453-65100454	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs141688611	chr11:65100471-65100472	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs200082256	chr11:65100473-65100474	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs577760288	chr11:65100480-65100481	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs540028843	chr11:65100486-65100487	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs35922774	chr11:65100488-65100489	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs560326975	chr11:65100489-65100490	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs573828022	chr11:65100494-65100495	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs12577028	chr11:65100502-65100503	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs12222749	chr11:65100504-65100505	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs12574891	chr11:65100506-65100507	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs36039888	chr11:65100507-65100508	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs12225450	chr11:65100508-65100509	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs12577030	chr11:65100516-65100517	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs199960633	chr11:65100518-65100519	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs12222750	chr11:65100520-65100521	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs12225451	chr11:65100522-65100523	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs12222752	chr11:65100528-65100529	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	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
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Chronic lymphocytic leukemia	22228453	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65085000-65100800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:65085200-65101000	Weak transcription	Fetal Kidney	kidney
3	chr11:65085800-65101000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:65088800-65101000	Weak transcription	Right Atrium	heart
5	chr11:65089200-65101000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr11:65089400-65101200	Weak transcription	Small Intestine	intestine
7	chr11:65089800-65100800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr11:65089800-65101000	Weak transcription	Liver	Liver
9	chr11:65089800-65101000	Weak transcription	Esophagus	oesophagus
10	chr11:65090000-65101000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:65090000-65101000	Weak transcription	Brain Substantia Nigra	brain
12	chr11:65090000-65101000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr11:65090200-65100800	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr11:65090200-65100800	Weak transcription	Colonic Mucosa	Colon
15	chr11:65090200-65101000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:65090200-65101000	Weak transcription	Fetal Lung	lung
17	chr11:65090200-65101000	Weak transcription	Rectal Smooth Muscle	rectum
18	chr11:65090400-65101000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr11:65090400-65101000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:65090400-65101000	Weak transcription	Left Ventricle	heart
21	chr11:65090400-65101000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr11:65090400-65101000	Weak transcription	HSMM	muscle
23	chr11:65090600-65101000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr11:65091800-65101000	Weak transcription	HSMMtube	muscle
25	chr11:65094200-65100800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr11:65096200-65100800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:65096200-65101000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr11:65097200-65101000	Weak transcription	Fetal Brain Male	brain
29	chr11:65097400-65100800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr11:65097400-65100800	Weak transcription	Stomach Smooth Muscle	stomach
31	chr11:65097400-65100800	Weak transcription	Osteobl	bone
32	chr11:65097400-65101000	Weak transcription	Duodenum Mucosa	Duodenum
33	chr11:65097400-65101000	Weak transcription	NHLF	lung
34	chr11:65097600-65100600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr11:65097600-65100800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr11:65097600-65100800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:65097600-65100800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:65097600-65100800	Weak transcription	Fetal Brain Female	brain
39	chr11:65097600-65100800	Weak transcription	Fetal Intestine Large	intestine
40	chr11:65097600-65100800	Weak transcription	Fetal Stomach	stomach
41	chr11:65097600-65100800	Weak transcription	Hela-S3	cervix
42	chr11:65097600-65101000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr11:65097600-65101000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr11:65097600-65101000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr11:65097600-65101000	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr11:65097600-65101000	Weak transcription	Brain Angular Gyrus	brain
47	chr11:65097600-65101000	Weak transcription	Brain Anterior Caudate	brain
48	chr11:65097600-65101000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr11:65097600-65101000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr11:65097600-65101000	Weak transcription	Colon Smooth Muscle	Colon

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