Variant report

Variant	esv33724
Chromosome Location	chr6:31114473-31118573
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11)
CpG islands
(count:184)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:11 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:31117481-31117518	Kidney_OC	kidney:	n/a	n/a
2	CTCF	chr6:31115898-31115981	GM12878	blood:	n/a	n/a
3	POLR2A	chr6:31117173-31117637	HepG2	liver:	n/a	n/a
4	POLR2A	chr6:31118480-31118489	K562	blood:	n/a	n/a
5	POLR2A	chr6:31118182-31118215	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr6:31118500-31118517	K562	blood:	n/a	n/a
7	POLR2A	chr6:31117088-31117171	K562	blood:	n/a	n/a
8	POLR2A	chr6:31118262-31118322	K562	blood:	n/a	n/a
9	POLR2A	chr6:31118351-31118359	K562	blood:	n/a	n/a
10	RUNX3	chr6:31116036-31116312	GM12878	blood:	n/a	n/a
11	RUNX3	chr6:31115992-31116340	GM12878	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31116343-31116393	NB4	blood:	n/a
2	chr6:31116343-31116393	NB4	blood:	n/a
3	chr6:31117380-31117430	PANC-1	pancreas:	n/a
4	chr6:31116343-31116393	BJ	skin:	n/a
5	chr6:31116408-31116458	Hela-S3	cervix:	n/a
6	chr6:31116408-31116458	PFSK-1	brain:	n/a
7	chr6:31116343-31116393	K562	blood:	n/a
8	chr6:31116343-31116393	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:31117380-31117430	HCF	heart:	n/a
10	chr6:31116343-31116393	AG09319	gingival:	n/a
11	chr6:31117380-31117430	AG09319	gingival:	n/a
12	chr6:31117380-31117430	NB4	blood:	n/a
13	chr6:31116343-31116393	U87	brain:	n/a
14	chr6:31116408-31116458	AG09309	skin:	n/a
15	chr6:31116343-31116393	A549	lung:	n/a
16	chr6:31116408-31116458	GM19239	blood:	n/a
17	chr6:31116408-31116458	NT2-D1	testis:	n/a
18	chr6:31116408-31116458	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:31116408-31116458	SK-N-MC	brain:	n/a
20	chr6:31116408-31116458	AoSMC	blood vessel:	n/a
21	chr6:31116343-31116393	AG04449	skin:	fetal
22	chr6:31117380-31117430	HAEpiC	amniotic membrane:	n/a
23	chr6:31116408-31116458	HRCEpiC	kidney:	n/a
24	chr6:31116408-31116458	Hepatocyte	liver:	n/a
25	chr6:31117380-31117430	Hela-S3	cervix:	n/a
26	chr6:31116408-31116458	HEK293	kidney:	embryo
27	chr6:31116408-31116458	CMK	blood:	n/a
28	chr6:31116343-31116393	LNCaP	prostate:	n/a
29	chr6:31117380-31117430	BJ	skin:	n/a
30	chr6:31117380-31117430	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:31117380-31117430	HNPCEpiC	eye:	n/a
32	chr6:31116408-31116458	A549	lung:	n/a
33	chr6:31116408-31116458	MCF-7	breast:	n/a
34	chr6:31117380-31117430	SK-N-SH_RA	brain:	n/a
35	chr6:31117380-31117430	AG04450	lung:	fetal
36	chr6:31116408-31116458	HRPEpiC	eye:	n/a
37	chr6:31116343-31116393	HEEpiC	esophagus:	n/a
38	chr6:31116408-31116458	BJ	skin:	n/a
39	chr6:31116343-31116393	ProgFib	skin:	n/a
40	chr6:31116343-31116393	PANC-1	pancreas:	n/a
41	chr6:31116408-31116458	AG04449	skin:	fetal
42	chr6:31116408-31116458	GM12891	blood:	n/a
43	chr6:31116343-31116393	SK-N-SH_RA	brain:	n/a
44	chr6:31116343-31116393	HRPEpiC	eye:	n/a
45	chr6:31116343-31116393	NH-A	brain:	n/a
46	chr6:31116408-31116458	BE2_C	brain:	n/a
47	chr6:31117380-31117430	HRCEpiC	kidney:	n/a
48	chr6:31116343-31116393	HCT-116	colon:	n/a
49	chr6:31117380-31117430	MCF10A-Er-Src	breast:	n/a
50	chr6:31116343-31116393	HepG2	liver:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31111544..31114466-chr6:31118106..31119797,2	MCF-7	breast:
2	chr6:31107129..31110169-chr6:31111741..31115408,4	K562	blood:
3	chr6:31107022..31110169-chr6:31112293..31115408,4	K562	blood:
4	chr6:31110527..31114153-chr6:31115554..31119425,5	K562	blood:
5	chr6:31116689..31119145-chr6:31122656..31125188,2	K562	blood:
6	chr6:31108839..31114213-chr6:31117147..31120721,5	K562	blood:
7	chr6:31114677..31116707-chr6:31122128..31124910,2	K562	blood:
8	chr6:31112475..31116177-chr6:31122128..31126125,5	K562	blood:
9	chr6:31105124..31107713-chr6:31116298..31118063,2	K562	blood:
10	chr6:31117081..31119149-chr6:31125462..31127055,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POU5F1-9	chr6:31116937-31117445	NONHSAT108728

No data

Variant related genes	Relation type
CCHCR1	TF binding region
CCHCR1	CpG island
ENSG00000204536	chromatin interactions
ENSG00000238211	chromatin interactions
ENSG00000204540	chromatin interactions
ENSG00000137310	chromatin interactions
ENSG00000204538	chromatin interactions

Extended variants
information (count: 170 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:170 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545501387	chr6:31114479-31114480	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs9263749	chr6:31114515-31114516	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs2240064	chr6:31114573-31114574	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs543166710	chr6:31114590-31114591	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs550738196	chr6:31114640-31114641	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs372189139	chr6:31114642-31114643	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs9263750	chr6:31114655-31114656	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs9263751	chr6:31114724-31114725	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs562491232	chr6:31114731-31114732	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs2240063	chr6:31114745-31114746	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs2240062	chr6:31114762-31114763	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs566193924	chr6:31114772-31114773	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs12523890	chr6:31114820-31114821	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs549112835	chr6:31114826-31114827	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs555361164	chr6:31114834-31114835	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs117335980	chr6:31114846-31114847	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs2240061	chr6:31114848-31114849	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs1265071	chr6:31114855-31114856	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs2240060	chr6:31114900-31114901	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs539006745	chr6:31114916-31114917	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs554217916	chr6:31114921-31114922	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs572526805	chr6:31114936-31114937	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs548178797	chr6:31114955-31114956	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs138598988	chr6:31115032-31115033	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs537252505	chr6:31115084-31115085	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs59878855	chr6:31115112-31115113	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs148870053	chr6:31115164-31115165	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs576520475	chr6:31115177-31115178	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs142527460	chr6:31115187-31115188	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs199962679	chr6:31115190-31115191	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs57243444	chr6:31115194-31115195	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs540045873	chr6:31115198-31115199	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138225273	chr6:31115205-31115206	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs1265070	chr6:31115207-31115208	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs113735362	chr6:31115209-31115210	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs6903261	chr6:31115307-31115308	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs544561256	chr6:31115352-31115353	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs572337748	chr6:31115432-31115433	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs3131012	chr6:31115441-31115442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs186288001	chr6:31115575-31115576	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs548843237	chr6:31115601-31115602	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs3131013	chr6:31115604-31115605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs9263756	chr6:31115655-31115656	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs538937502	chr6:31115712-31115713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs567731777	chr6:31115726-31115727	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547890167	chr6:31115770-31115771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532105612	chr6:31115775-31115776	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs569590938	chr6:31115818-31115819	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559341375	chr6:31115844-31115845	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190714909	chr6:31115852-31115853	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Ovarian cancer	21781307	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31105600-31124400	Weak transcription	Fetal Kidney	kidney
2	chr6:31105600-31124800	Weak transcription	Small Intestine	intestine
3	chr6:31105800-31117000	Weak transcription	Brain Substantia Nigra	brain
4	chr6:31105800-31117200	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr6:31105800-31117800	Weak transcription	Primary B cells from cord blood	blood
6	chr6:31105800-31121800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr6:31105800-31122600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:31105800-31124400	Weak transcription	Colon Smooth Muscle	Colon
9	chr6:31105800-31124800	Weak transcription	Hela-S3	cervix
10	chr6:31105800-31125200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr6:31106000-31125000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr6:31106000-31125000	Weak transcription	Fetal Brain Male	brain
13	chr6:31106000-31125200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:31107600-31125000	Weak transcription	NHDF-Ad	bronchial
15	chr6:31107800-31117200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:31107800-31125000	Weak transcription	Fetal Heart	heart
17	chr6:31108000-31116200	Weak transcription	Esophagus	oesophagus
18	chr6:31109800-31114800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr6:31110000-31124600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr6:31110200-31114600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:31110200-31114600	Strong transcription	Brain Anterior Caudate	brain
22	chr6:31110200-31114800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:31110200-31117200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:31110200-31125000	Weak transcription	A549	lung
25	chr6:31110400-31114800	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr6:31110600-31117800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr6:31110800-31117000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:31110800-31117800	Weak transcription	HepG2	liver
29	chr6:31111000-31114800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:31111000-31116000	Weak transcription	Brain Angular Gyrus	brain
31	chr6:31111000-31116200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:31111000-31118800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:31111000-31121800	Weak transcription	K562	blood
34	chr6:31111000-31124400	Weak transcription	Psoas Muscle	Psoas
35	chr6:31111000-31125000	Weak transcription	NHEK	skin
36	chr6:31111000-31125200	Weak transcription	HSMMtube	muscle
37	chr6:31111200-31114600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:31111200-31125000	Weak transcription	HUVEC	blood vessel
39	chr6:31111400-31114600	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr6:31111400-31116000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr6:31111400-31117200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr6:31111400-31117600	Weak transcription	HSMM	muscle
43	chr6:31111400-31119600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr6:31111400-31124400	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:31111400-31124800	Weak transcription	Aorta	Aorta
46	chr6:31111400-31124800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr6:31111400-31124800	Strong transcription	Fetal Stomach	stomach
48	chr6:31111400-31125000	Weak transcription	Right Atrium	heart
49	chr6:31111400-31125000	Weak transcription	HMEC	breast
50	chr6:31111400-31125600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links