Variant report

Variant	esv3390320
Chromosome Location	chr6:5134378-5136926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:201)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:201 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr6:5136052-5136178	HepG2	liver:	n/a	n/a
2	CTCF	chr6:5135874-5136453	HCT-116	colon:	n/a	n/a
3	CTCF	chr6:5135992-5136301	K562	blood:	n/a	n/a
4	CTCF	chr6:5136120-5136270	BE2_C	brain:	n/a	n/a
5	CTCF	chr6:5136104-5136352	GM19240	blood:	n/a	n/a
6	CTCF	chr6:5136160-5136310	GM12864	blood:	n/a	n/a
7	CTCF	chr6:5136100-5136250	HRPEpiC	eye:	n/a	n/a
8	CTCF	chr6:5135987-5136397	GM12878	blood:	n/a	n/a
9	CTCF	chr6:5136080-5136230	HRPEpiC	eye:	n/a	n/a
10	CTCF	chr6:5136120-5136270	HFF-Myc	foreskin:	n/a	n/a
11	CTCF	chr6:5136100-5136250	GM12866	blood:	n/a	n/a
12	CTCF	chr6:5136073-5136324	HepG2	liver:	n/a	n/a
13	CTCF	chr6:5136085-5136318	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr6:5136160-5136310	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr6:5136120-5136270	GM12875	blood:	n/a	n/a
16	CTCF	chr6:5136120-5136270	K562	blood:	n/a	n/a
17	CTCF	chr6:5136400-5136550	GM12875	blood:	n/a	n/a
18	CTCF	chr6:5136068-5136343	MCF-7	breast:	n/a	n/a
19	CTCF	chr6:5136080-5136230	GM12866	blood:	n/a	n/a
20	CTCF	chr6:5136180-5136330	MCF-7	breast:	n/a	n/a
21	CTCF	chr6:5136140-5136290	HRE	kidney:	n/a	n/a
22	CTCF	chr6:5136105-5136314	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:5136053-5136270	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr6:5136089-5136325	GM10266	blood:	n/a	n/a
25	CTCF	chr6:5136140-5136290	SAEC	small airway:	n/a	n/a
26	CTCF	chr6:5136067-5136336	K562	blood:	n/a	n/a
27	CTCF	chr6:5136080-5136230	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr6:5136059-5136379	A549	lung:	n/a	n/a
29	CTCF	chr6:5136100-5136250	HCFaa	heart:	n/a	n/a
30	CTCF	chr6:5136140-5136290	BE2_C	brain:	n/a	n/a
31	CTCF	chr6:5136080-5136230	HCT-116	colon:	n/a	n/a
32	CTCF	chr6:5136107-5136280	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:5136100-5136321	Fibrobl	skin:	n/a	n/a
34	CTCF	chr6:5135188-5135253	Lung_OC	lung:	n/a	n/a
35	CTCF	chr6:5136160-5136310	GM06990	blood:	n/a	n/a
36	CTCF	chr6:5136045-5136377	K562	blood:	n/a	n/a
37	CTCF	chr6:5136120-5136270	GM12870	blood:	n/a	n/a
38	CTCF	chr6:5136095-5136262	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr6:5136060-5136210	GM12871	blood:	n/a	n/a
40	CTCF	chr6:5136069-5136320	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr6:5136140-5136290	NHEK	skin:	n/a	n/a
42	CTCF	chr6:5136120-5136270	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr6:5136100-5136250	Caco-2	colon:	n/a	n/a
44	CTCF	chr6:5136120-5136270	AG09319	gingival:	n/a	n/a
45	CTCF	chr6:5136022-5136381	IMR90	lung:	n/a	n/a
46	CTCF	chr6:5136120-5136270	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr6:5136120-5136270	AG10803	skin:	n/a	n/a
48	CTCF	chr6:5136078-5136298	GM13977	blood:	n/a	n/a
49	CTCF	chr6:5136160-5136310	GM12875	blood:	n/a	n/a
50	CTCF	chr6:5135847-5136641	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5136301-5136351	Hela-S3	cervix:	n/a
2	chr6:5135794-5135844	HCT-116	colon:	n/a
3	chr6:5135794-5135844	HNPCEpiC	eye:	n/a
4	chr6:5136301-5136351	ovcar-3	ovarian:	n/a
5	chr6:5136301-5136351	Caco-2	colon:	n/a
6	chr6:5136301-5136351	HEEpiC	esophagus:	n/a
7	chr6:5136301-5136351	MCF10A-Er-Src	breast:	n/a
8	chr6:5135794-5135844	HEEpiC	esophagus:	n/a
9	chr6:5135794-5135844	MCF10A-Er-Src	breast:	n/a
10	chr6:5135794-5135844	U87	brain:	n/a
11	chr6:5135184-5135234	HEEpiC	esophagus:	n/a
12	chr6:5136301-5136351	AG04450	lung:	fetal
13	chr6:5136301-5136351	GM19239	blood:	n/a
14	chr6:5136301-5136351	NHDF-neo	bronchial:	n/a
15	chr6:5135184-5135234	GM19239	blood:	n/a
16	chr6:5136301-5136351	SK-N-SH	brain:	n/a
17	chr6:5135794-5135844	HCPEpiC	choroid plexus:	n/a
18	chr6:5135794-5135844	Hela-S3	cervix:	n/a
19	chr6:5135184-5135234	HCPEpiC	choroid plexus:	n/a
20	chr6:5135794-5135844	NHDF-neo	bronchial:	n/a
21	chr6:5135794-5135844	GM12878	blood:	n/a
22	chr6:5135184-5135234	SK-N-SH	brain:	n/a
23	chr6:5135794-5135844	A549	lung:	n/a
24	chr6:5136301-5136351	H1-hESC	embryonic stem cell:	embryo
25	chr6:5135794-5135844	T-47D	breast:	n/a
26	chr6:5136301-5136351	LNCaP	prostate:	n/a
27	chr6:5135184-5135234	T-47D	breast:	n/a
28	chr6:5135184-5135234	Caco-2	colon:	n/a
29	chr6:5136301-5136351	GM12891	blood:	n/a
30	chr6:5136301-5136351	PANC-1	pancreas:	n/a
31	chr6:5135794-5135844	NHBE	bronchial:	n/a
32	chr6:5135794-5135844	NH-A	brain:	n/a
33	chr6:5136301-5136351	HMEC	breast:	n/a
34	chr6:5135794-5135844	HUVEC	blood vessel:	n/a
35	chr6:5135794-5135844	SK-N-MC	brain:	n/a
36	chr6:5136301-5136351	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:5136301-5136351	PrEC	prostate:	n/a
38	chr6:5135184-5135234	HRE	kidney:	n/a
39	chr6:5136301-5136351	NH-A	brain:	n/a
40	chr6:5136301-5136351	U87	brain:	n/a
41	chr6:5135794-5135844	AoSMC	blood vessel:	n/a
42	chr6:5136301-5136351	GM12892	blood:	n/a
43	chr6:5135794-5135844	HL-60	blood:	n/a
44	chr6:5136301-5136351	BJ	skin:	n/a
45	chr6:5135184-5135234	NHBE	bronchial:	n/a
46	chr6:5135184-5135234	GM12878	blood:	n/a
47	chr6:5135794-5135844	HIPEpiC	eye:	n/a
48	chr6:5135794-5135844	GM12891	blood:	n/a
49	chr6:5135794-5135844	ProgFib	skin:	n/a
50	chr6:5136301-5136351	SKMC	muscle:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:5056866..5057674-chr6:5135884..5136820,3	MCF-7	breast:
2	chr6:5135691..5136262-chr6:5402310..5402817,2	K562	blood:

No data

Variant related genes	Relation type
LYRM4	TF binding region
LYRM4	CpG island

Extended variants
information (count: 138 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:138 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56935942	chr6:5134386-5134387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545429373	chr6:5134458-5134459	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs113137588	chr6:5134462-5134463	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs412628	chr6:5134496-5134497	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs423801	chr6:5134504-5134505	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs561924958	chr6:5134523-5134524	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs424006	chr6:5134574-5134575	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs364886	chr6:5134592-5134593	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs569209089	chr6:5134613-5134614	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs369878629	chr6:5134628-5134629	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs533345907	chr6:5134677-5134678	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs142207990	chr6:5134680-5134681	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs373405718	chr6:5134738-5134739	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs454984	chr6:5134763-5134764	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs534312145	chr6:5134832-5134833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12192863	chr6:5134858-5134859	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs58060009	chr6:5134877-5134878	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs372990497	chr6:5134917-5134918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs193244727	chr6:5134938-5134939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113500548	chr6:5135028-5135029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577945518	chr6:5135067-5135068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75910094	chr6:5135075-5135076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145944148	chr6:5135076-5135077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377555120	chr6:5135079-5135080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs683261	chr6:5135120-5135121	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs557371072	chr6:5135126-5135127	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs566475026	chr6:5135128-5135129	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs531936902	chr6:5135129-5135130	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs585956	chr6:5135156-5135157	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs585970	chr6:5135160-5135161	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs183674433	chr6:5135176-5135177	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs585998	chr6:5135179-5135180	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs73717674	chr6:5135184-5135185	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs113846353	chr6:5135188-5135189	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs73717675	chr6:5135212-5135213	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs562770485	chr6:5135229-5135230	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs111823365	chr6:5135240-5135241	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs373639851	chr6:5135260-5135261	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs188623445	chr6:5135268-5135269	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs71547285	chr6:5135272-5135273	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs575838029	chr6:5135278-5135279	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs71547286	chr6:5135288-5135289	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs71547287	chr6:5135291-5135292	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs192331787	chr6:5135296-5135297	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs586517	chr6:5135300-5135301	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185237694	chr6:5135306-5135307	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs560672545	chr6:5135314-5135315	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs13220253	chr6:5135316-5135317	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs650785	chr6:5135319-5135320	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs111806223	chr6:5135328-5135329	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5128800-5136200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr6:5129000-5136800	Weak transcription	Primary T cells from cord blood	blood
3	chr6:5129000-5162000	Weak transcription	K562	blood
4	chr6:5129800-5138000	Weak transcription	HepG2	liver
5	chr6:5130600-5140400	Weak transcription	Gastric	stomach
6	chr6:5130600-5172200	Weak transcription	Lung	lung
7	chr6:5130800-5139400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:5130800-5142400	Weak transcription	Fetal Intestine Small	intestine
9	chr6:5131000-5143000	Weak transcription	Spleen	Spleen
10	chr6:5131800-5134400	Enhancers	Primary B cells from peripheral blood	blood
11	chr6:5131800-5135200	Weak transcription	Placenta	Placenta
12	chr6:5132000-5134600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:5132000-5139200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:5132200-5134400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr6:5132200-5134400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr6:5132600-5134600	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr6:5133000-5134400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr6:5133200-5141800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr6:5133400-5134400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr6:5133400-5134800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr6:5133400-5135200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr6:5133400-5136600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr6:5133400-5143200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:5133400-5143800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr6:5133400-5144000	Weak transcription	Fetal Brain Male	brain
26	chr6:5133400-5146000	Weak transcription	Psoas Muscle	Psoas
27	chr6:5133400-5151600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr6:5133600-5134600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr6:5133600-5134600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr6:5133600-5136600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:5133600-5143400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr6:5133600-5143800	Weak transcription	Fetal Stomach	stomach
33	chr6:5133800-5134600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:5133800-5134600	Enhancers	Adipose Nuclei	Adipose
35	chr6:5133800-5136200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr6:5133800-5136200	Weak transcription	Brain Anterior Caudate	brain
37	chr6:5133800-5136200	Weak transcription	HUVEC	blood vessel
38	chr6:5133800-5139200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr6:5133800-5139400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:5133800-5140000	Weak transcription	GM12878-XiMat	blood
41	chr6:5133800-5140600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:5133800-5142400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:5133800-5143000	Weak transcription	Fetal Muscle Leg	muscle
44	chr6:5133800-5143400	Weak transcription	Left Ventricle	heart
45	chr6:5133800-5143600	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr6:5133800-5153400	Weak transcription	Right Ventricle	heart
47	chr6:5134000-5134800	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr6:5134000-5135800	Enhancers	NHEK	skin
49	chr6:5134200-5135000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:5134200-5135800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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