Variant report

Variant	nsv1045170
Chromosome Location	chr13:110815422-110836716
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	BACH1	chr13:110830246-110830455	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:110830189-110830479	K562	blood:	n/a	n/a
3	CEBPB	chr13:110827167-110827235	HepG2	liver:	n/a	chr13:110827200-110827211 chr13:110827198-110827209 chr13:110827200-110827211
4	CEBPB	chr13:110815635-110815945	A549	lung:	n/a	chr13:110815794-110815807
5	CEBPB	chr13:110815706-110815986	H1-hESC	embryonic stem cell:	n/a	chr13:110815794-110815807
6	CEBPB	chr13:110815626-110815965	IMR90	lung:	n/a	chr13:110815794-110815807
7	CEBPB	chr13:110815736-110815851	Hela-S3	cervix:	n/a	chr13:110815794-110815807
8	CEBPB	chr13:110815634-110815974	HepG2	liver:	n/a	chr13:110815794-110815807
9	CTCF	chr13:110816160-110816310	Caco-2	colon:	n/a	n/a
10	CTCF	chr13:110830320-110830470	SAEC	small airway:	n/a	n/a
11	CTCF	chr13:110832640-110832790	HBMEC	blood vessel:	n/a	chr13:110832727-110832745 chr13:110832727-110832736
12	CTCF	chr13:110833040-110833190	GM12869	blood:	n/a	n/a
13	E2F4	chr13:110816617-110816795	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr13:110813003-110816105	SK-N-SH	brain:	n/a	chr13:110815476-110815490
15	EP300	chr13:110831952-110832257	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr13:110835717-110836916	SK-N-SH	brain:	n/a	n/a
17	EP300	chr13:110836358-110836608	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr13:110815329-110815680	SK-N-SH_RA	brain:	n/a	chr13:110815476-110815490
19	FOS	chr13:110825900-110826082	MCF10A-Er-Src	breast:	n/a	chr13:110825988-110825996 chr13:110825991-110825999
20	FOS	chr13:110825824-110826101	MCF10A-Er-Src	breast:	n/a	chr13:110825988-110825996 chr13:110825991-110825999
21	FOS	chr13:110825899-110826108	MCF10A-Er-Src	breast:	n/a	chr13:110825988-110825996 chr13:110825991-110825999
22	FOS	chr13:110825813-110826123	MCF10A-Er-Src	breast:	n/a	chr13:110825988-110825996 chr13:110825991-110825999
23	FOS	chr13:110819121-110819243	MCF10A-Er-Src	breast:	n/a	n/a
24	GATA2	chr13:110836031-110836679	SH-SY5Y	brain:	n/a	chr13:110836098-110836111
25	GATA2	chr13:110815356-110815826	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr13:110815412-110815747	SH-SY5Y	brain:	n/a	n/a
27	GTF2F1	chr13:110819759-110819805	Hela-S3	cervix:	n/a	n/a
28	JUND	chr13:110825846-110826106	H1-hESC	embryonic stem cell:	n/a	chr13:110825988-110825996 chr13:110825991-110825999
29	MAFF	chr13:110819007-110819248	HepG2	liver:	n/a	chr13:110819156-110819174
30	MAFF	chr13:110830188-110830425	K562	blood:	n/a	chr13:110830328-110830346
31	MAFF	chr13:110830215-110830506	HepG2	liver:	n/a	chr13:110830328-110830346
32	MAFK	chr13:110830193-110830459	IMR90	lung:	n/a	chr13:110830335-110830345 chr13:110830331-110830342 chr13:110830330-110830341 chr13:110830330-110830345 chr13:110830331-110830342 chr13:110830335-110830344 chr13:110830330-110830341
33	MAFK	chr13:110819015-110819323	HepG2	liver:	n/a	chr13:110819157-110819172
34	MAFK	chr13:110830181-110830497	HepG2	liver:	n/a	chr13:110830335-110830345 chr13:110830331-110830342 chr13:110830330-110830341 chr13:110830330-110830345 chr13:110830331-110830342 chr13:110830335-110830344 chr13:110830330-110830341
35	MAFK	chr13:110830290-110830457	K562	blood:	n/a	chr13:110830335-110830345 chr13:110830331-110830342 chr13:110830330-110830341 chr13:110830330-110830345 chr13:110830331-110830342 chr13:110830335-110830344 chr13:110830330-110830341
36	MAFK	chr13:110830186-110830466	HepG2	liver:	n/a	chr13:110830335-110830345 chr13:110830331-110830342 chr13:110830330-110830341 chr13:110830330-110830345 chr13:110830331-110830342 chr13:110830335-110830344 chr13:110830330-110830341
37	MAFK	chr13:110819027-110819291	HepG2	liver:	n/a	chr13:110819157-110819172
38	MAFK	chr13:110831767-110831783	HepG2	liver:	n/a	n/a
39	MAFK	chr13:110819000-110819315	IMR90	lung:	n/a	chr13:110819157-110819172
40	MAFK	chr13:110819056-110819235	Hela-S3	cervix:	n/a	chr13:110819157-110819172
41	MAX	chr13:110815291-110815567	NB4	blood:	n/a	chr13:110815312-110815319 chr13:110815311-110815320 chr13:110815382-110815391 chr13:110815311-110815320
42	MXI1	chr13:110813482-110815891	SK-N-SH	brain:	n/a	n/a
43	MYC	chr13:110815321-110815449	NB4	blood:	n/a	chr13:110815382-110815391
44	POLR2A	chr13:110822744-110822774	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr13:110832801-110832811	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr13:110828459-110828501	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr13:110835673-110835932	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr13:110820331-110820465	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr13:110817792-110817935	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr13:110832170-110832299	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:110832764-110832814	ECC-1	luminal epithelium:	n/a
2	chr13:110832764-110832814	AG10803	skin:	n/a
3	chr13:110832764-110832814	K562	blood:	n/a
4	chr13:110832764-110832814	CMK	blood:	n/a
5	chr13:110835673-110835723	CMK	blood:	n/a
6	chr13:110832764-110832814	NB4	blood:	n/a
7	chr13:110832764-110832814	BJ	skin:	n/a
8	chr13:110835673-110835723	GM12878	blood:	n/a
9	chr13:110835709-110835759	AG04449	skin:	fetal
10	chr13:110832764-110832814	PANC-1	pancreas:	n/a
11	chr13:110832764-110832814	HNPCEpiC	eye:	n/a
12	chr13:110835673-110835723	U87	brain:	n/a
13	chr13:110835709-110835759	NHDF-neo	bronchial:	n/a
14	chr13:110835673-110835723	Caco-2	colon:	n/a
15	chr13:110835709-110835759	AG04450	lung:	fetal
16	chr13:110832764-110832814	GM06990	blood:	n/a
17	chr13:110835709-110835759	HAEpiC	amniotic membrane:	n/a
18	chr13:110835673-110835723	MCF-7	breast:	n/a
19	chr13:110832764-110832814	Jurkat	blood:	n/a
20	chr13:110835709-110835759	U87	brain:	n/a
21	chr13:110835673-110835723	IMR90	lung:	fetal
22	chr13:110835709-110835759	HIPEpiC	eye:	n/a
23	chr13:110835709-110835759	HNPCEpiC	eye:	n/a
24	chr13:110835673-110835723	HEEpiC	esophagus:	n/a
25	chr13:110835709-110835759	IMR90	lung:	fetal
26	chr13:110835709-110835759	AoSMC	blood vessel:	n/a
27	chr13:110835673-110835723	T-47D	breast:	n/a
28	chr13:110832764-110832814	HepG2	liver:	n/a
29	chr13:110835709-110835759	ECC-1	luminal epithelium:	n/a
30	chr13:110835709-110835759	Jurkat	blood:	n/a
31	chr13:110835673-110835723	HIPEpiC	eye:	n/a
32	chr13:110832764-110832814	HCT-116	colon:	n/a
33	chr13:110835709-110835759	CMK	blood:	n/a
34	chr13:110835709-110835759	SAEC	small airway:	n/a
35	chr13:110835709-110835759	HPAEpiC	pulmonary alveolar:	n/a
36	chr13:110835673-110835723	NB4	blood:	n/a
37	chr13:110835709-110835759	HEEpiC	esophagus:	n/a
38	chr13:110835709-110835759	HCPEpiC	choroid plexus:	n/a
39	chr13:110832764-110832814	ovcar-3	ovarian:	n/a
40	chr13:110835673-110835723	NH-A	brain:	n/a
41	chr13:110835673-110835723	HMEC	breast:	n/a
42	chr13:110835673-110835723	GM19239	blood:	n/a
43	chr13:110835673-110835723	HRCEpiC	kidney:	n/a
44	chr13:110835673-110835723	Jurkat	blood:	n/a
45	chr13:110832764-110832814	SK-N-SH	brain:	n/a
46	chr13:110835709-110835759	HepG2	liver:	n/a
47	chr13:110835709-110835759	HCF	heart:	n/a
48	chr13:110835709-110835759	HMEC	breast:	n/a
49	chr13:110835709-110835759	Hepatocyte	liver:	n/a
50	chr13:110835673-110835723	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:110826571..110829024-chr13:110829639..110833128,3	K562	blood:
2	chr13:110826571..110829024-chr13:110829639..110833128,3	K562	blood:

Variant related genes	Relation type
COL4A1	TF binding region
COL4A1	CpG island

Extended variants
information (count: 1058 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547174304	chr13:110815434-110815435	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144495645	chr13:110815447-110815448	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148035572	chr13:110815558-110815559	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113485024	chr13:110815596-110815597	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs367678017	chr13:110815614-110815615	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549291992	chr13:110815616-110815617	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2298240	chr13:110815673-110815674	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs538113369	chr13:110815751-110815752	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376224472	chr13:110815760-110815761	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372602087	chr13:110815779-110815780	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551567717	chr13:110815782-110815783	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183228479	chr13:110815788-110815789	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370943043	chr13:110815789-110815790	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186028417	chr13:110815801-110815802	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374682248	chr13:110815804-110815805	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190543628	chr13:110815818-110815819	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368879632	chr13:110815820-110815821	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368150613	chr13:110815825-110815826	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200734000	chr13:110815830-110815831	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372976488	chr13:110815838-110815839	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs141714960	chr13:110815856-110815857	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs182728431	chr13:110815892-110815893	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs150594280	chr13:110815917-110815918	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs112561721	chr13:110815928-110815929	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs369407797	chr13:110815943-110815944	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572139999	chr13:110815968-110815969	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs541156336	chr13:110816007-110816008	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs192850661	chr13:110816018-110816019	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs529712012	chr13:110816021-110816022	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs549378904	chr13:110816038-110816039	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs16975426	chr13:110816040-110816041	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs199618882	chr13:110816060-110816061	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs386774672	chr13:110816062-110816063	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs531886343	chr13:110816063-110816064	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs146941348	chr13:110816073-110816074	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs2298241	chr13:110816097-110816098	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs113777564	chr13:110816107-110816108	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534111231	chr13:110816125-110816126	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139644011	chr13:110816131-110816132	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs60279490	chr13:110816143-110816144	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs536704754	chr13:110816144-110816145	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564415668	chr13:110816279-110816280	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556603404	chr13:110816295-110816296	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs116018908	chr13:110816306-110816307	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs201067974	chr13:110816307-110816308	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs371851693	chr13:110816315-110816316	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201382782	chr13:110816332-110816333	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs56215481	chr13:110816337-110816338	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200599709	chr13:110816347-110816348	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs58236306	chr13:110816353-110816354	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110791200-110825600	Weak transcription	Esophagus	oesophagus
2	chr13:110791400-110820800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr13:110791400-110825800	Weak transcription	A549	lung
4	chr13:110791400-110868400	Weak transcription	Psoas Muscle	Psoas
5	chr13:110795800-110826000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr13:110798400-110825400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:110798800-110825600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:110798800-110853200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr13:110799000-110821200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr13:110799600-110840200	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr13:110800000-110824800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:110800000-110825800	Strong transcription	Ovary	ovary
13	chr13:110800200-110837800	Strong transcription	NH-A	brain
14	chr13:110800600-110834200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr13:110800800-110821800	Strong transcription	Placenta	Placenta
16	chr13:110801000-110818400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr13:110801000-110822600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr13:110802400-110822000	Strong transcription	Colon Smooth Muscle	Colon
19	chr13:110802400-110842800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr13:110803000-110822000	Weak transcription	Small Intestine	intestine
21	chr13:110803000-110834200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr13:110803000-110840400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr13:110803200-110815800	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr13:110803200-110826000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr13:110803200-110839800	Weak transcription	NHDF-Ad	bronchial
26	chr13:110803200-110839800	Strong transcription	Osteobl	bone
27	chr13:110803600-110840000	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr13:110804000-110825800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr13:110804800-110825200	Weak transcription	Brain Anterior Caudate	brain
30	chr13:110806200-110824000	Weak transcription	Liver	Liver
31	chr13:110806600-110860400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr13:110807800-110826200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr13:110808000-110824000	Weak transcription	Colonic Mucosa	Colon
34	chr13:110809000-110821400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr13:110809000-110822000	Strong transcription	Fetal Muscle Trunk	muscle
36	chr13:110809200-110821200	Strong transcription	Fetal Lung	lung
37	chr13:110809200-110840000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr13:110809400-110817000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr13:110809400-110824800	Weak transcription	Fetal Brain Female	brain
40	chr13:110809600-110828000	Weak transcription	Fetal Brain Male	brain
41	chr13:110809800-110816400	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr13:110809800-110819800	Strong transcription	Fetal Intestine Large	intestine
43	chr13:110809800-110820200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr13:110809800-110820600	Strong transcription	Fetal Stomach	stomach
45	chr13:110809800-110831200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr13:110810200-110866400	Strong transcription	Stomach Smooth Muscle	stomach
47	chr13:110810400-110826000	Strong transcription	Aorta	Aorta
48	chr13:110810600-110825600	Weak transcription	Brain Cingulate Gyrus	brain
49	chr13:110810800-110819600	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr13:110810800-110824000	Strong transcription	Lung	lung

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