Variant report

Variant	nsv515732
Chromosome Location	chr6:24705835-24709830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:216 , 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	BCL3	chr6:24708763-24709246	A549	lung:	n/a	n/a
2	BCLAF1	chr6:24708910-24710048	K562	blood:	n/a	n/a
3	BCLAF1	chr6:24708975-24709615	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:24705911-24705986	GM12878	blood:	n/a	n/a
5	CCNT2	chr6:24709187-24709483	K562	blood:	n/a	n/a
6	CEBPB	chr6:24708175-24708312	K562	blood:	n/a	chr6:24708189-24708200
7	CEBPB	chr6:24708179-24708237	HepG2	liver:	n/a	chr6:24708189-24708200
8	CEBPB	chr6:24707218-24707250	K562	blood:	n/a	n/a
9	EP300	chr6:24709192-24709330	K562	blood:	n/a	chr6:24709244-24709258
10	HEY1	chr6:24709294-24709825	HepG2	liver:	n/a	n/a
11	HMGN3	chr6:24708240-24708433	K562	blood:	n/a	n/a
12	IRF3	chr6:24709246-24709392	GM12878	blood:	n/a	chr6:24709284-24709293
13	MAFK	chr6:24707157-24707171	K562	blood:	n/a	n/a
14	MAFK	chr6:24709205-24709255	K562	blood:	n/a	n/a
15	MBD4	chr6:24708854-24709800	HepG2	liver:	n/a	n/a
16	MTA3	chr6:24708824-24709794	GM12878	blood:	n/a	n/a
17	NFATC1	chr6:24707304-24707763	GM12878	blood:	n/a	n/a
18	NFATC1	chr6:24708844-24709697	GM12878	blood:	n/a	n/a
19	NFATC1	chr6:24708790-24709902	GM12878	blood:	n/a	n/a
20	PML	chr6:24708908-24710168	K562	blood:	n/a	n/a
21	PML	chr6:24708755-24709838	GM12878	blood:	n/a	n/a
22	POLR2A	chr6:24708947-24708969	ProgFib	skin:	n/a	n/a
23	POLR2A	chr6:24707553-24707753	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr6:24705928-24706519	MCF-7	breast:	n/a	n/a
25	POLR2A	chr6:24708722-24709691	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr6:24709216-24709223	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr6:24707218-24707995	K562	blood:	n/a	n/a
28	POLR2A	chr6:24706919-24707114	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr6:24708484-24708884	K562	blood:	n/a	n/a
30	POLR2A	chr6:24709265-24709902	K562	blood:	n/a	n/a
31	POLR2A	chr6:24707422-24708023	K562	blood:	n/a	n/a
32	POLR2A	chr6:24708215-24708887	GM12892	blood:	n/a	n/a
33	POLR2A	chr6:24707447-24707989	HL-60	blood:	n/a	n/a
34	POLR2A	chr6:24705616-24710087	A549	lung:	n/a	n/a
35	POLR2A	chr6:24706913-24707935	SK-N-SH	brain:	n/a	n/a
36	POLR2A	chr6:24708728-24709512	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr6:24709262-24709523	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr6:24705773-24706168	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr6:24708192-24708422	SK-N-SH	brain:	n/a	n/a
40	POLR2A	chr6:24707408-24707964	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr6:24699666-24722345	K562	blood:	n/a	n/a
42	POLR2A	chr6:24707328-24707972	GM12892	blood:	n/a	n/a
43	POLR2A	chr6:24707005-24707126	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr6:24709774-24709906	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr6:24707357-24707631	GM12891	blood:	n/a	n/a
46	POLR2A	chr6:24708858-24709119	GM12878	blood:	n/a	n/a
47	POLR2A	chr6:24707583-24707825	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr6:24709262-24709497	U87	brain:	n/a	n/a
49	POLR2A	chr6:24708381-24708518	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr6:24707439-24707554	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:24706172-24706222	PrEC	prostate:	n/a
2	chr6:24706172-24706222	GM12892	blood:	n/a
3	chr6:24706172-24706222	T-47D	breast:	n/a
4	chr6:24706172-24706222	MCF10A-Er-Src	breast:	n/a
5	chr6:24706172-24706222	CMK	blood:	n/a
6	chr6:24706172-24706222	BJ	skin:	n/a
7	chr6:24706172-24706222	HCF	heart:	n/a
8	chr6:24706172-24706222	HRE	kidney:	n/a
9	chr6:24706172-24706222	AG04450	lung:	fetal
10	chr6:24706172-24706222	IMR90	lung:	fetal
11	chr6:24706172-24706222	AG09319	gingival:	n/a
12	chr6:24706172-24706222	MCF-7	breast:	n/a
13	chr6:24706172-24706222	HEK293	kidney:	embryo
14	chr6:24706172-24706222	H1-hESC	embryonic stem cell:	embryo
15	chr6:24706172-24706222	SK-N-SH_RA	brain:	n/a
16	chr6:24706172-24706222	Hela-S3	cervix:	n/a
17	chr6:24706172-24706222	A549	lung:	n/a
18	chr6:24706172-24706222	SKMC	muscle:	n/a
19	chr6:24706172-24706222	NT2-D1	testis:	n/a
20	chr6:24706172-24706222	NB4	blood:	n/a
21	chr6:24706172-24706222	Jurkat	blood:	n/a
22	chr6:24706172-24706222	HepG2	liver:	n/a
23	chr6:24706172-24706222	NH-A	brain:	n/a
24	chr6:24706172-24706222	AG10803	skin:	n/a
25	chr6:24706172-24706222	GM12878	blood:	n/a
26	chr6:24706172-24706222	AG09309	skin:	n/a
27	chr6:24706172-24706222	HEEpiC	esophagus:	n/a
28	chr6:24706172-24706222	SK-N-SH	brain:	n/a
29	chr6:24706172-24706222	BE2_C	brain:	n/a
30	chr6:24706172-24706222	ProgFib	skin:	n/a
31	chr6:24706172-24706222	GM12891	blood:	n/a
32	chr6:24706172-24706222	Hepatocyte	liver:	n/a
33	chr6:24706172-24706222	AG04449	skin:	fetal
34	chr6:24706172-24706222	K562	blood:	n/a
35	chr6:24706172-24706222	HAEpiC	amniotic membrane:	n/a
36	chr6:24706172-24706222	HCT-116	colon:	n/a
37	chr6:24706172-24706222	SK-N-MC	brain:	n/a
38	chr6:24706172-24706222	Caco-2	colon:	n/a
39	chr6:24706172-24706222	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:24706172-24706222	GM19239	blood:	n/a
41	chr6:24706172-24706222	HIPEpiC	eye:	n/a
42	chr6:24706172-24706222	HRCEpiC	kidney:	n/a
43	chr6:24706172-24706222	NHDF-neo	bronchial:	n/a
44	chr6:24706172-24706222	U87	brain:	n/a
45	chr6:24706172-24706222	AoSMC	blood vessel:	n/a
46	chr6:24706172-24706222	SAEC	small airway:	n/a
47	chr6:24706172-24706222	HL-60	blood:	n/a
48	chr6:24706172-24706222	ovcar-3	ovarian:	n/a
49	chr6:24706172-24706222	NHBE	bronchial:	n/a
50	chr6:24706172-24706222	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:24706431..24709046-chr6:24773872..24777096,3	K562	blood:
2	chr6:24701974..24704901-chr6:24705179..24706820,2	K562	blood:
3	chr6:24700062..24702859-chr6:24704909..24709163,3	MCF-7	breast:
4	chr6:24703121..24705782-chr6:24707406..24711144,3	MCF-7	breast:
5	chr6:24697429..24699456-chr6:24708438..24711427,3	K562	blood:
6	chr6:24704323..24706405-chr6:24780403..24782969,2	K562	blood:
7	chr6:24707645..24711659-chr6:24779375..24784848,6	K562	blood:
8	chr6:24705180..24707870-chr6:24773614..24775393,3	K562	blood:
9	chr6:24666486..24669007-chr6:24703954..24705943,2	MCF-7	breast:
10	chr6:24709253..24711356-chr6:24713475..24715005,2	MCF-7	breast:
11	chr6:24696748..24707740-chr6:24716503..24724189,24	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOT13-1	chr6:24706975-24707379	ENSG00000272402.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C6orf62	hsa-miR-93-5p	chr6:24706292-24706314

Variant related genes	Relation type
ENSG00000272402	TF binding region
ENSG00000272345	TF binding region
ENSG00000272402	CpG island
ENSG00000272345	CpG island
ENSG00000112304	chromatin interactions
ENSG00000272345	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000111802	chromatin interactions
ENSG00000112312	chromatin interactions

Extended variants
information (count: 211 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:211 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3756814	chr6:24705835-24705836	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531877792	chr6:24705861-24705862	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs568797257	chr6:24705909-24705910	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs548373908	chr6:24705918-24705919	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs561981681	chr6:24705920-24705921	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs527898705	chr6:24705922-24705923	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs547559957	chr6:24705935-24705936	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs148118403	chr6:24705937-24705938	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs376109685	chr6:24705999-24706000	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs191178386	chr6:24706056-24706057	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs542891220	chr6:24706112-24706113	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs536031605	chr6:24706166-24706167	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs539704869	chr6:24706173-24706174	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs552192482	chr6:24706175-24706176	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs568759130	chr6:24706177-24706178	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs560875955	chr6:24706182-24706183	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs183035063	chr6:24706250-24706251	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs115365615	chr6:24706278-24706279	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs550859079	chr6:24706355-24706356	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs377415125	chr6:24706371-24706372	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs374287394	chr6:24706385-24706386	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs372450488	chr6:24706388-24706389	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs145980580	chr6:24706402-24706403	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs9358794	chr6:24706416-24706417	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs139875623	chr6:24706452-24706453	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs149237704	chr6:24706469-24706470	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs202045794	chr6:24706486-24706487	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs201218708	chr6:24706496-24706497	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs555999137	chr6:24706497-24706498	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs569455277	chr6:24706554-24706555	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs185799918	chr6:24706606-24706607	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs190993026	chr6:24706612-24706613	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs542174733	chr6:24706685-24706686	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs183350060	chr6:24706712-24706713	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs6931809	chr6:24706770-24706771	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs541235932	chr6:24706776-24706777	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs149738850	chr6:24706817-24706818	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs533729430	chr6:24706839-24706840	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs550190141	chr6:24706848-24706849	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs6909099	chr6:24706852-24706853	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs144643620	chr6:24706898-24706899	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs548161046	chr6:24706915-24706916	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs148485705	chr6:24706918-24706919	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs115367909	chr6:24706928-24706929	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs554054627	chr6:24706930-24706931	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs142600817	chr6:24706960-24706961	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs147615448	chr6:24706961-24706962	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs188628563	chr6:24706993-24706994	Strong transcription Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs576261197	chr6:24707047-24707048	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs541864699	chr6:24707075-24707076	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	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
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
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24684800-24709000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:24696600-24710400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr6:24697800-24715800	Strong transcription	Fetal Thymus	thymus
4	chr6:24698000-24711600	Strong transcription	Primary T cells from cord blood	blood
5	chr6:24698200-24716200	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr6:24698200-24716200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:24698200-24716400	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:24698200-24717400	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:24698400-24706000	Weak transcription	Fetal Brain Male	brain
10	chr6:24698400-24717400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:24698600-24715200	Weak transcription	Fetal Heart	heart
12	chr6:24698600-24716200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr6:24698600-24716200	Weak transcription	Right Atrium	heart
14	chr6:24699000-24716600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:24699000-24717400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:24699600-24712800	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr6:24699800-24712400	Strong transcription	Dnd41	blood
18	chr6:24700000-24716800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:24700200-24713200	Weak transcription	Stomach Mucosa	stomach
20	chr6:24700600-24712400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr6:24700800-24707800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr6:24701000-24707000	Weak transcription	Gastric	stomach
23	chr6:24701000-24711400	Strong transcription	Brain Hippocampus Middle	brain
24	chr6:24701200-24710600	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr6:24701200-24711400	Strong transcription	Liver	Liver
26	chr6:24701200-24712200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr6:24701200-24713000	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr6:24701200-24714200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:24701400-24711000	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr6:24701400-24711400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:24701400-24712200	Strong transcription	Duodenum Mucosa	Duodenum
32	chr6:24701400-24713000	Strong transcription	Primary B cells from cord blood	blood
33	chr6:24701400-24713000	Strong transcription	Primary hematopoietic stem cells	blood
34	chr6:24701400-24713200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:24701400-24713200	Strong transcription	Fetal Intestine Large	intestine
36	chr6:24701400-24715400	Strong transcription	Rectal Mucosa Donor 31	rectum
37	chr6:24701400-24716800	Strong transcription	Placenta	Placenta
38	chr6:24701600-24712000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr6:24701600-24712400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr6:24701600-24714800	Strong transcription	HUVEC	blood vessel
41	chr6:24701600-24716200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr6:24701600-24716200	Strong transcription	Stomach Smooth Muscle	stomach
43	chr6:24701600-24716200	Strong transcription	HMEC	breast
44	chr6:24701600-24716600	Strong transcription	Fetal Muscle Trunk	muscle
45	chr6:24701600-24716600	Strong transcription	Fetal Muscle Leg	muscle
46	chr6:24701800-24706000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:24701800-24706200	Weak transcription	Esophagus	oesophagus
48	chr6:24701800-24715400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr6:24701800-24715600	Strong transcription	Osteobl	bone
50	chr6:24701800-24716200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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