Variant report

Variant	nsv900578
Chromosome Location	chr13:76136976-76167433
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	chr13:76140823-76141209	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:76140888-76140979	K562	blood:	n/a	n/a
3	ATF2	chr13:76161744-76162155	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr13:76161743-76162267	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:76152548-76152550	K562	blood:	n/a	n/a
6	BATF	chr13:76153753-76153938	GM12878	blood:	n/a	n/a
7	BATF	chr13:76153723-76153987	GM12878	blood:	n/a	n/a
8	BRCA1	chr13:76153639-76153677	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr13:76159288-76159637	K562	blood:	n/a	n/a
10	CBX3	chr13:76159335-76159585	K562	blood:	n/a	n/a
11	CEBPB	chr13:76140737-76141073	IMR90	lung:	n/a	n/a
12	CEBPB	chr13:76140760-76141096	A549	lung:	n/a	n/a
13	CEBPB	chr13:76140756-76141122	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr13:76164922-76165193	IMR90	lung:	n/a	chr13:76165016-76165027
15	CEBPB	chr13:76140781-76141013	K562	blood:	n/a	n/a
16	CEBPB	chr13:76161851-76162197	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr13:76164885-76165156	K562	blood:	n/a	chr13:76165016-76165027
18	CEBPB	chr13:76164903-76165196	HepG2	liver:	n/a	chr13:76165016-76165027
19	CEBPB	chr13:76161789-76162201	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:76140742-76141072	HepG2	liver:	n/a	n/a
21	CTCF	chr13:76140980-76141130	AG09309	skin:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
22	CTCF	chr13:76140960-76141110	HL-60	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
23	CTCF	chr13:76140920-76141070	BJ	skin:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
24	CTCF	chr13:76141020-76141170	GM12864	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
25	CTCF	chr13:76140980-76141130	GM12873	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
26	CTCF	chr13:76140960-76141110	HCPEpiC	choroid plexus:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
27	CTCF	chr13:76140998-76141148	Lung_OC	lung:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
28	CTCF	chr13:76160331-76160405	Lung_OC	lung:	n/a	n/a
29	CTCF	chr13:76140940-76141090	HBMEC	blood vessel:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
30	CTCF	chr13:76140960-76141110	NHDF-neo	bronchial:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
31	CTCF	chr13:76140789-76141348	A549	lung:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
32	CTCF	chr13:76140980-76141130	HCT-116	colon:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
33	CTCF	chr13:76140940-76141090	GM12872	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
34	CTCF	chr13:76141020-76141170	HCPEpiC	choroid plexus:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
35	CTCF	chr13:76140960-76141110	HUVEC	blood vessel:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
36	CTCF	chr13:76140945-76141133	GM13977	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
37	CTCF	chr13:76140980-76141130	AG09319	gingival:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
38	CTCF	chr13:76140958-76141129	GM10266	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
39	CTCF	chr13:76140940-76141090	SK-N-SH_RA	brain:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
40	CTCF	chr13:76140920-76141070	GM12878	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
41	CTCF	chr13:76140882-76141218	K562	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
42	CTCF	chr13:76140940-76141090	GM12868	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
43	CTCF	chr13:76140940-76141090	HRPEpiC	eye:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
44	CTCF	chr13:76140908-76141172	HUVEC	blood vessel:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
45	CTCF	chr13:76140960-76141110	HPAF	blood vessel:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
46	CTCF	chr13:76141000-76141117	GM20000	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
47	CTCF	chr13:76140960-76141110	HRPEpiC	eye:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
48	CTCF	chr13:76140940-76141090	Hela-S3	cervix:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
49	CTCF	chr13:76140960-76141110	GM12873	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
50	CTCF	chr13:76140980-76140999	Gliobla	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:76160277..76161808-chr13:76162172..76164407,2	K562	blood:
2	chr13:76143405..76146053-chr13:76147700..76149492,2	K562	blood:
3	chr13:76153049..76155664-chr13:76161169..76162949,2	K562	blood:
4	chr13:76152309..76155041-chr13:76158108..76159629,2	K562	blood:
5	chr13:76141660..76144515-chr13:76144732..76146608,2	MCF-7	breast:
6	chr13:76123286..76125327-chr13:76160450..76162067,2	K562	blood:
7	chr13:76152309..76155041-chr13:76158108..76159629,2	K562	blood:
8	chr13:76123475..76126296-chr13:76136199..76138617,2	MCF-7	breast:
9	chr13:76124076..76125593-chr13:76162284..76165016,2	K562	blood:
10	chr13:76153049..76155664-chr13:76161169..76162949,2	K562	blood:
11	chr13:76160277..76161808-chr13:76162172..76164407,2	K562	blood:
12	chr13:76143405..76146053-chr13:76147700..76149492,2	K562	blood:
13	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LMO7-2	chr13:76140968-76140987	ENSG00000261553.1
2	lnc-LMO7-2	chr13:76141363-76141448	ENSG00000261553.1
3	lnc-LMO7-2	chr13:76143596-76143643	ENSG00000261553.1
4	lnc-COMMD6-4	chr13:76161358-76161715	l_873_chr13:76072523-76201534_testes
5	lnc-COMMD6-4	chr13:76140115-76140230	l_873_chr13:76072523-76201534_testes

Variant related genes	Relation type
ENSG00000261553	TF binding region
UCHL3	TF binding region
ENSG00000118939	chromatin interactions
ENSG00000261553	chromatin interactions
ENSG00000188243	chromatin interactions

Extended variants
information (count: 1076 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1076 , 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	rs9543977	chr13:76136976-76136977	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181912309	chr13:76136980-76136981	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs141425477	chr13:76137039-76137040	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs529741170	chr13:76137074-76137075	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs541939440	chr13:76137075-76137076	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs562941628	chr13:76137130-76137131	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs185748683	chr13:76137132-76137133	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs188982613	chr13:76137140-76137141	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs181887128	chr13:76137169-76137170	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs5804820	chr13:76137180-76137181	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs186552269	chr13:76137214-76137215	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs576761811	chr13:76137262-76137263	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs67532728	chr13:76137263-76137264	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs546462641	chr13:76137287-76137288	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs375625755	chr13:76137291-76137292	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs28659861	chr13:76137295-76137296	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs9543978	chr13:76137303-76137304	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs577341467	chr13:76137314-76137315	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs555399105	chr13:76137351-76137352	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs574003187	chr13:76137365-76137366	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs555083133	chr13:76137378-76137379	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs570023998	chr13:76137417-76137418	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs537443765	chr13:76137430-76137431	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs559268012	chr13:76137437-76137438	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs541035844	chr13:76137505-76137506	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs150814669	chr13:76137636-76137637	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs541747256	chr13:76137706-76137707	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs553272842	chr13:76137711-76137712	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs565597901	chr13:76137716-76137717	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs530176242	chr13:76137740-76137741	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs56868157	chr13:76137741-76137742	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs138344990	chr13:76137764-76137765	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs191309191	chr13:76137885-76137886	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs144094499	chr13:76137946-76137947	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs182770749	chr13:76137958-76137959	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs4885312	chr13:76138044-76138045	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148195198	chr13:76138056-76138057	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs552120652	chr13:76138057-76138058	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs58677064	chr13:76138079-76138080	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs61959729	chr13:76138080-76138081	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs61959730	chr13:76138082-76138083	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs185377794	chr13:76138165-76138166	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs562777663	chr13:76138211-76138212	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs546920108	chr13:76138257-76138258	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568150079	chr13:76138269-76138270	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs117603542	chr13:76138289-76138290	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs35022480	chr13:76138291-76138292	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs71127557	chr13:76138298-76138299	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs80122107	chr13:76138303-76138304	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs77099327	chr13:76138304-76138305	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:848 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76124600-76183000	Weak transcription	Small Intestine	intestine
2	chr13:76124800-76146400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr13:76124800-76146600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr13:76124800-76146600	Weak transcription	Lung	lung
5	chr13:76124800-76147600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:76124800-76164000	Weak transcription	Spleen	Spleen
7	chr13:76124800-76167600	Weak transcription	Gastric	stomach
8	chr13:76124800-76170600	Weak transcription	Colonic Mucosa	Colon
9	chr13:76125000-76141400	Weak transcription	Fetal Lung	lung
10	chr13:76125000-76143400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr13:76125000-76147600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr13:76125000-76156200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr13:76125000-76158000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr13:76125000-76192800	Weak transcription	Brain Substantia Nigra	brain
15	chr13:76125000-76209600	Weak transcription	Right Ventricle	heart
16	chr13:76125200-76141000	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr13:76125200-76147200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr13:76125200-76147200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr13:76125200-76147600	Weak transcription	Brain Angular Gyrus	brain
20	chr13:76125200-76173800	Weak transcription	Fetal Heart	heart
21	chr13:76125200-76177800	Weak transcription	Stomach Mucosa	stomach
22	chr13:76125400-76138800	Weak transcription	Fetal Intestine Small	intestine
23	chr13:76125400-76143000	Weak transcription	Brain Hippocampus Middle	brain
24	chr13:76125400-76143000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr13:76125400-76143200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr13:76125400-76147000	Weak transcription	Brain Germinal Matrix	brain
27	chr13:76125400-76147600	Weak transcription	Brain Anterior Caudate	brain
28	chr13:76125400-76191000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr13:76125600-76158000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr13:76125600-76182000	Weak transcription	Fetal Brain Male	brain
31	chr13:76126600-76140200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr13:76128200-76143800	Weak transcription	NHLF	lung
33	chr13:76129400-76143800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr13:76129400-76145000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr13:76129400-76145800	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr13:76129400-76147200	Weak transcription	Aorta	Aorta
37	chr13:76129400-76147200	Weak transcription	Left Ventricle	heart
38	chr13:76129400-76147600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr13:76129400-76151400	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr13:76129400-76158000	Weak transcription	Fetal Kidney	kidney
41	chr13:76129400-76180400	Weak transcription	Thymus	Thymus
42	chr13:76129600-76137200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:76129600-76137200	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr13:76129600-76141400	Weak transcription	Adipose Nuclei	Adipose
45	chr13:76129600-76141400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr13:76129600-76141400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr13:76129600-76141400	Weak transcription	Fetal Muscle Leg	muscle
48	chr13:76129600-76143600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr13:76129600-76143600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr13:76129600-76144000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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