Variant report

Variant	nsv526110
Chromosome Location	chr6:30800577-30810654
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 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	BHLHE40	chr6:30809671-30809940	GM12878	blood:	n/a	n/a
2	BHLHE40	chr6:30808460-30808697	K562	blood:	n/a	n/a
3	BHLHE40	chr6:30809999-30810311	K562	blood:	n/a	n/a
4	BRCA1	chr6:30804205-30804632	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr6:30809812-30810343	K562	blood:	n/a	n/a
6	CCNT2	chr6:30810104-30810257	K562	blood:	n/a	n/a
7	CCNT2	chr6:30808811-30808882	K562	blood:	n/a	n/a
8	CEBPB	chr6:30804057-30804700	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr6:30804037-30804764	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr6:30807560-30807691	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:30804124-30804318	HepG2	liver:	n/a	n/a
12	CEBPB	chr6:30804024-30804690	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr6:30804234-30804545	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr6:30809040-30809190	BE2_C	brain:	n/a	n/a
15	CTCF	chr6:30806200-30806350	GM12874	blood:	n/a	n/a
16	CTCF	chr6:30802440-30802590	GM12871	blood:	n/a	n/a
17	CTCF	chr6:30806235-30806313	GM12878	blood:	n/a	n/a
18	CTCF	chr6:30806080-30806230	HAc	cerebellar:	n/a	n/a
19	CTCF	chr6:30801220-30801370	GM12875	blood:	n/a	n/a
20	CTCF	chr6:30806360-30806510	GM12873	blood:	n/a	n/a
21	CUX1	chr6:30800614-30801022	K562	blood:	n/a	n/a
22	E2F6	chr6:30808944-30809843	H1-hESC	embryonic stem cell:	n/a	n/a
23	E2F6	chr6:30806008-30807154	H1-hESC	embryonic stem cell:	n/a	n/a
24	EBF1	chr6:30809931-30810058	GM12878	blood:	n/a	n/a
25	EBF1	chr6:30809062-30809690	GM12878	blood:	n/a	n/a
26	EP300	chr6:30810115-30810123	GM12878	blood:	n/a	n/a
27	EP300	chr6:30803973-30804849	ECC-1	luminal epithelium:	n/a	chr6:30804544-30804558
28	EP300	chr6:30809550-30810094	GM12878	blood:	n/a	n/a
29	EP300	chr6:30805589-30805929	SK-N-SH_RA	brain:	n/a	chr6:30805889-30805896
30	EP300	chr6:30806101-30806383	H1-hESC	embryonic stem cell:	n/a	n/a
31	EP300	chr6:30805525-30805881	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr6:30804123-30804739	Hela-S3	cervix:	n/a	chr6:30804544-30804558
33	EP300	chr6:30806289-30806363	GM12878	blood:	n/a	n/a
34	EP300	chr6:30809486-30810120	GM12878	blood:	n/a	n/a
35	EP300	chr6:30809873-30810318	K562	blood:	n/a	n/a
36	EP300	chr6:30804032-30804660	ECC-1	luminal epithelium:	n/a	chr6:30804544-30804558
37	ESR1	chr6:30804147-30804609	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr6:30804237-30804608	ECC-1	luminal epithelium:	n/a	n/a
39	ESR1	chr6:30804174-30804666	ECC-1	luminal epithelium:	n/a	n/a
40	ESR1	chr6:30804250-30804573	ECC-1	luminal epithelium:	n/a	n/a
41	ESR1	chr6:30804169-30804672	ECC-1	luminal epithelium:	n/a	n/a
42	FOS	chr6:30804296-30804436	MCF10A-Er-Src	breast:	n/a	n/a
43	FOXA2	chr6:30807574-30807865	A549	lung:	n/a	n/a
44	FOXM1	chr6:30804052-30804784	ECC-1	luminal epithelium:	n/a	n/a
45	GATA1	chr6:30809915-30810257	PBDE	blood:	n/a	n/a
46	GATA1	chr6:30809858-30810448	K562	blood:	n/a	n/a
47	GATA3	chr6:30809956-30810250	T-47D	breast:	n/a	n/a
48	GTF2F1	chr6:30806122-30806999	H1-hESC	embryonic stem cell:	n/a	n/a
49	GTF2F1	chr6:30809982-30810034	H1-hESC	embryonic stem cell:	n/a	n/a
50	GTF2F1	chr6:30804152-30804546	Hela-S3	cervix:	n/a	n/a

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30707567..30712185-chr6:30801298..30803959,4	MCF-7	breast:
2	chr6:30710179..30712517-chr6:30808321..30811657,4	MCF-7	breast:
3	chr6:30800474..30806072-chr6:30842215..30847924,9	K562	blood:
4	chr6:30708712..30711147-chr6:30810186..30812455,3	K562	blood:
5	chr6:30809749..30812115-chr6:30849210..30852847,3	MCF-7	breast:
6	chr6:30798389..30801828-chr6:30850243..30854490,5	MCF-7	breast:
7	chr6:30800474..30803474-chr6:30842113..30845625,4	K562	blood:
8	chr6:30805834..30810192-chr6:30850275..30853725,4	MCF-7	breast:
9	chr6:30806333..30810243-chr6:30843203..30846067,3	K562	blood:
10	chr6:30799998..30802555-chr6:30804287..30805987,2	MCF-7	breast:
11	chr6:30810334..30813136-chr6:30813626..30816587,2	K562	blood:
12	chr6:30800550..30802804-chr6:30880832..30883659,2	K562	blood:
13	chr6:30800305..30802395-chr6:30802717..30804530,3	K562	blood:
14	chr6:30803676..30806179-chr6:30849399..30852097,2	MCF-7	breast:
15	chr6:30709350..30712510-chr6:30802787..30805110,3	MCF-7	breast:
16	chr6:30807490..30810871-chr6:30840456..30844706,4	MCF-7	breast:
17	chr6:30703666..30722133-chr6:30776009..30801352,184	MCF-7	breast:
18	chr6:30799998..30802555-chr6:30804287..30805987,2	MCF-7	breast:
19	chr6:30800305..30802395-chr6:30802717..30804530,3	K562	blood:
20	chr6:30807490..30809248-chr6:30824608..30826344,2	MCF-7	breast:
21	chr6:30780598..30803497-chr6:30842531..30855110,80	MCF-7	breast:
22	chr6:30793601..30795460-chr6:30804124..30806213,2	K562	blood:
23	chr6:30806007..30809728-chr6:30842937..30845561,3	K562	blood:
24	chr6:30807003..30808509-chr6:30812271..30813825,2	K562	blood:
25	chr6:30800606..30802983-chr6:30909821..30912255,2	K562	blood:
26	chr6:30796516..30799472-chr6:30801979..30805833,4	MCF-7	breast:
27	chr6:30796462..30798109-chr6:30809712..30812488,2	K562	blood:
28	chr6:30807011..30808968-chr6:30850726..30853143,2	MCF-7	breast:
29	chr6:30780643..30783504-chr6:30803282..30805852,2	K562	blood:
30	chr6:30582567..30584748-chr6:30808358..30810776,3	MCF-7	breast:
31	chr6:30582933..30584813-chr6:30802694..30804722,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SFTA2-12	chr6:30807303-30807796	XLOC_005675
2	lnc-DDR1-4	chr6:30806046-30806451	NONHSAT108683
3	lnc-SFTA2-12	chr6:30807638-30807796	XLOC_005675
4	lnc-SFTA2-12	chr6:30805173-30807796	NONHSAT108684

No data

Variant related genes	Relation type
LINC00243	TF binding region
ENSG00000137411	chromatin interactions
ENSG00000201988	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000237775	chromatin interactions
ENSG00000204580	chromatin interactions
ENSG00000214894	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000263608	chromatin interactions
ENSG00000237923	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 335 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535395798	chr6:30800614-30800615	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs369485438	chr6:30800615-30800616	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs143144519	chr6:30800687-30800688	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs568691986	chr6:30800696-30800697	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs138793507	chr6:30800706-30800707	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs576297587	chr6:30800728-30800729	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs554337765	chr6:30800733-30800734	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs543299242	chr6:30800755-30800756	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs564768077	chr6:30800781-30800782	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs577439986	chr6:30800835-30800836	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs116097605	chr6:30800847-30800848	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs142904801	chr6:30800851-30800852	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs147442990	chr6:30800860-30800861	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs540795529	chr6:30800870-30800871	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs374191502	chr6:30800879-30800880	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs532219644	chr6:30800889-30800890	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs530058915	chr6:30800902-30800903	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs559973241	chr6:30800913-30800914	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs200744545	chr6:30800926-30800927	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs201764091	chr6:30800927-30800928	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs78392797	chr6:30800929-30800930	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs139756074	chr6:30801056-30801057	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs540915343	chr6:30801126-30801127	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs563917970	chr6:30801135-30801136	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs532897980	chr6:30801137-30801138	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs368214426	chr6:30801138-30801139	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs6930910	chr6:30801141-30801142	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs546726674	chr6:30801162-30801163	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs563016900	chr6:30801173-30801174	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs528886972	chr6:30801199-30801200	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs150608554	chr6:30801204-30801205	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs139798484	chr6:30801213-30801214	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs115442246	chr6:30801260-30801261	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs117713987	chr6:30801443-30801444	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs568691883	chr6:30801444-30801445	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs548042177	chr6:30801538-30801539	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs117054911	chr6:30801542-30801543	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs540008112	chr6:30801568-30801569	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs371580231	chr6:30801645-30801646	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs556695841	chr6:30801752-30801753	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs188338183	chr6:30801760-30801761	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs376687433	chr6:30801795-30801796	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs572278881	chr6:30801809-30801810	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs566944566	chr6:30801857-30801858	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs146366928	chr6:30801867-30801868	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs577438951	chr6:30801894-30801895	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs139652837	chr6:30801949-30801950	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs369662187	chr6:30802013-30802014	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs1264342	chr6:30802017-30802018	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs370126275	chr6:30802027-30802028	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
Lung cancer	21569311	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30796200-30805600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:30796200-30805600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:30796400-30805200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:30796400-30805400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:30796800-30802200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:30796800-30802200	Weak transcription	HSMM	muscle
7	chr6:30796800-30802400	Weak transcription	Right Atrium	heart
8	chr6:30796800-30804000	Weak transcription	Fetal Heart	heart
9	chr6:30796800-30804000	Weak transcription	Fetal Lung	lung
10	chr6:30796800-30804400	Weak transcription	Brain Hippocampus Middle	brain
11	chr6:30796800-30811000	Weak transcription	Right Ventricle	heart
12	chr6:30797000-30802200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:30797000-30802200	Weak transcription	Osteobl	bone
14	chr6:30797000-30804000	Weak transcription	Adipose Nuclei	Adipose
15	chr6:30797000-30804000	Weak transcription	Left Ventricle	heart
16	chr6:30797000-30808400	Weak transcription	Esophagus	oesophagus
17	chr6:30797200-30804000	Weak transcription	Psoas Muscle	Psoas
18	chr6:30797200-30812000	Weak transcription	Lung	lung
19	chr6:30797600-30802200	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr6:30797600-30802200	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr6:30798000-30802400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr6:30798000-30805600	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr6:30798000-30805600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr6:30798000-30805600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr6:30798400-30802600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr6:30798400-30804000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr6:30798400-30804000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:30798400-30809000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr6:30798600-30802200	Enhancers	Fetal Thymus	thymus
30	chr6:30798800-30801200	Enhancers	Dnd41	blood
31	chr6:30798800-30802000	Weak transcription	Primary B cells from peripheral blood	blood
32	chr6:30798800-30802200	Weak transcription	K562	blood
33	chr6:30798800-30804000	Weak transcription	Fetal Muscle Leg	muscle
34	chr6:30798800-30805600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:30798800-30806200	Weak transcription	GM12878-XiMat	blood
36	chr6:30799000-30801000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr6:30799200-30801600	Weak transcription	Primary B cells from cord blood	blood
38	chr6:30799200-30812200	Weak transcription	Spleen	Spleen
39	chr6:30799400-30800600	Enhancers	Placenta Amnion	Placenta Amnion
40	chr6:30799400-30802200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr6:30799400-30803400	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr6:30799600-30800600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr6:30799600-30800600	Weak transcription	Thymus	Thymus
44	chr6:30799600-30801200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr6:30799600-30801200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr6:30799600-30802000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr6:30799600-30802200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr6:30799600-30802200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr6:30799600-30802400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:30799800-30800600	Enhancers	Placenta	Placenta

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