Variant report

Variant	nsv966836
Chromosome Location	chr7:66438146-66457576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:66440226-66440478	K562	blood:	n/a	n/a
2	BHLHE40	chr7:66440311-66440415	K562	blood:	n/a	n/a
3	CBX3	chr7:66445108-66445974	K562	blood:	n/a	n/a
4	CBX3	chr7:66445246-66445925	K562	blood:	n/a	n/a
5	CBX3	chr7:66440088-66440402	K562	blood:	n/a	n/a
6	CEBPB	chr7:66438158-66438418	K562	blood:	n/a	n/a
7	CEBPB	chr7:66440372-66440611	K562	blood:	n/a	n/a
8	CEBPB	chr7:66443979-66444393	IMR90	lung:	n/a	n/a
9	CEBPB	chr7:66438269-66438469	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:66449447-66449483	HepG2	liver:	n/a	chr7:66449464-66449475
11	CHD2	chr7:66440195-66440484	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr7:66440246-66440498	K562	blood:	n/a	n/a
13	CTCF	chr7:66444840-66444990	WI-38	lung:	n/a	n/a
14	CTCF	chr7:66445523-66445565	GM10266	blood:	n/a	n/a
15	CTCF	chr7:66451566-66451616	GM20000	blood:	n/a	n/a
16	CTCF	chr7:66456194-66456248	LNCaP	prostate:	n/a	n/a
17	CTCF	chr7:66454770-66454804	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr7:66457163-66457187	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr7:66444800-66444950	NHLF	lung:	n/a	n/a
20	CTCF	chr7:66444980-66445016	LNCaP	prostate:	n/a	n/a
21	CTCF	chr7:66457154-66457159	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr7:66452867-66452909	GM13976	blood:	n/a	n/a
23	CTCF	chr7:66444840-66444990	AG04450	lung:	n/a	n/a
24	EP300	chr7:66448692-66448856	GM12878	blood:	n/a	n/a
25	EP300	chr7:66440197-66440489	GM12878	blood:	n/a	n/a
26	EP300	chr7:66440178-66440664	K562	blood:	n/a	n/a
27	FOS	chr7:66440355-66440392	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr7:66440240-66440549	K562	blood:	n/a	n/a
29	HEY1	chr7:66456723-66456985	K562	blood:	n/a	n/a
30	HEY1	chr7:66440082-66440383	K562	blood:	n/a	n/a
31	HEY1	chr7:66454794-66455000	K562	blood:	n/a	n/a
32	HEY1	chr7:66457028-66457341	K562	blood:	n/a	n/a
33	IRF1	chr7:66440206-66440596	K562	blood:	n/a	n/a
34	IRF1	chr7:66457018-66457147	K562	blood:	n/a	n/a
35	IRF1	chr7:66457020-66457173	K562	blood:	n/a	n/a
36	IRF4	chr7:66445411-66445707	GM12878	blood:	n/a	n/a
37	JUND	chr7:66440178-66440517	K562	blood:	n/a	chr7:66440330-66440341
38	JUND	chr7:66440278-66440338	HepG2	liver:	n/a	n/a
39	KAP1	chr7:66445107-66445842	K562	blood:	n/a	n/a
40	MAFK	chr7:66453414-66453586	HepG2	liver:	n/a	n/a
41	MAX	chr7:66440340-66440374	HepG2	liver:	n/a	n/a
42	NFYA	chr7:66440240-66440593	K562	blood:	n/a	chr7:66440417-66440435
43	NFYB	chr7:66440271-66440542	Hela-S3	cervix:	n/a	chr7:66440343-66440358
44	NFYB	chr7:66440213-66440600	K562	blood:	n/a	chr7:66440343-66440358
45	PAX5	chr7:66445462-66445658	GM12878	blood:	n/a	n/a
46	POLR2A	chr7:66456810-66457309	A549	lung:	n/a	n/a
47	POLR2A	chr7:66453030-66453036	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr7:66440208-66440269	K562	blood:	n/a	n/a
49	POLR2A	chr7:66456639-66457246	GM12878	blood:	n/a	n/a
50	POLR2A	chr7:66451478-66451552	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66456737-66456787	AG04449	skin:	fetal
2	chr7:66456737-66456787	U87	brain:	n/a
3	chr7:66456737-66456787	MCF-7	breast:	n/a
4	chr7:66456737-66456787	HUVEC	blood vessel:	n/a
5	chr7:66456737-66456787	HRE	kidney:	n/a
6	chr7:66456737-66456787	HCM	heart:	n/a
7	chr7:66456737-66456787	SAEC	small airway:	n/a
8	chr7:66456737-66456787	NT2-D1	testis:	n/a
9	chr7:66456737-66456787	PANC-1	pancreas:	n/a
10	chr7:66456737-66456787	NHBE	bronchial:	n/a
11	chr7:66456737-66456787	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:66456737-66456787	AG10803	skin:	n/a
13	chr7:66456737-66456787	GM06990	blood:	n/a
14	chr7:66456737-66456787	HepG2	liver:	n/a
15	chr7:66456737-66456787	LNCaP	prostate:	n/a
16	chr7:66456737-66456787	A549	lung:	n/a
17	chr7:66456737-66456787	HIPEpiC	eye:	n/a
18	chr7:66456737-66456787	AoSMC	blood vessel:	n/a
19	chr7:66456737-66456787	RPTEC	kidney:	n/a
20	chr7:66456737-66456787	ProgFib	skin:	n/a
21	chr7:66456737-66456787	HEK293	kidney:	embryo
22	chr7:66456737-66456787	HAEpiC	amniotic membrane:	n/a
23	chr7:66456737-66456787	GM12892	blood:	n/a
24	chr7:66456737-66456787	Hepatocyte	liver:	n/a
25	chr7:66456737-66456787	NH-A	brain:	n/a
26	chr7:66456737-66456787	Hela-S3	cervix:	n/a
27	chr7:66456737-66456787	HRCEpiC	kidney:	n/a
28	chr7:66456737-66456787	AG04450	lung:	fetal
29	chr7:66456737-66456787	HCT-116	colon:	n/a
30	chr7:66456737-66456787	HEEpiC	esophagus:	n/a
31	chr7:66456737-66456787	BJ	skin:	n/a
32	chr7:66456737-66456787	NB4	blood:	n/a
33	chr7:66456737-66456787	ECC-1	luminal epithelium:	n/a
34	chr7:66456737-66456787	SK-N-SH	brain:	n/a
35	chr7:66456737-66456787	PrEC	prostate:	n/a
36	chr7:66456737-66456787	H1-hESC	embryonic stem cell:	embryo
37	chr7:66456737-66456787	Caco-2	colon:	n/a
38	chr7:66456737-66456787	HL-60	blood:	n/a
39	chr7:66456737-66456787	HCPEpiC	choroid plexus:	n/a
40	chr7:66456737-66456787	SK-N-SH_RA	brain:	n/a
41	chr7:66456737-66456787	NHDF-neo	bronchial:	n/a
42	chr7:66456737-66456787	SK-N-MC	brain:	n/a
43	chr7:66456737-66456787	PFSK-1	brain:	n/a
44	chr7:66456737-66456787	HCF	heart:	n/a
45	chr7:66456737-66456787	GM12891	blood:	n/a
46	chr7:66456737-66456787	MCF10A-Er-Src	breast:	n/a
47	chr7:66456737-66456787	K562	blood:	n/a
48	chr7:66456737-66456787	ovcar-3	ovarian:	n/a
49	chr7:66456737-66456787	BE2_C	brain:	n/a
50	chr7:66456737-66456787	CMK	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:66453405..66455098-chr7:66455519..66457456,2	MCF-7	breast:
2	chr7:66310807..66313244-chr7:66448820..66450934,2	MCF-7	breast:
3	chr7:66451976..66454311-chr7:66458213..66459754,2	K562	blood:
4	chr7:66448220..66451138-chr7:66454744..66456715,3	K562	blood:
5	chr7:66453405..66455098-chr7:66455519..66457456,2	MCF-7	breast:
6	chr7:66449461..66454980-chr7:66457220..66462076,6	K562	blood:
7	chr7:66430596..66433000-chr7:66437729..66440706,2	K562	blood:
8	chr7:66448220..66451138-chr7:66454744..66456715,3	K562	blood:
9	chr7:66447145..66450086-chr7:66451796..66453341,2	K562	blood:
10	chr7:66426423..66428356-chr7:66456046..66459032,2	K562	blood:
11	chr7:66425545..66427923-chr7:66455922..66457546,2	K562	blood:
12	chr7:66424823..66427121-chr7:66447406..66450272,2	K562	blood:
13	chr7:66447145..66450086-chr7:66451796..66453341,2	K562	blood:
14	chr7:66439219..66440739-chr8:101726060..101728497,2	MCF-7	breast:
15	chr7:66402496..66404175-chr7:66454564..66457521,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TYW1-2	chr7:66445107-66445395	NONHSAT121258
2	lnc-SBDS-1	chr7:66437995-66438201	XLOC_006483
3	lnc-SBDS-1	chr7:66440233-66440267	XLOC_006483
4	lnc-SBDS-1	chr7:66437995-66438201	XLOC_006483
5	lnc-SBDS-1	chr7:66440229-66440267	XLOC_006483

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SBDS	hsa-let-7c-5p	chr7:66453335-66453356
2	SBDS	hsa-miR-590-3p	chr7:66452723-66452743

Variant related genes	Relation type
TYW1	TF binding region
RN7SL43P	TF binding region
TYW1	CpG island
RN7SL43P	CpG island
ENSG00000198874	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000126524	chromatin interactions

Extended variants
information (count: 889 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:889 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139678318	chr7:66438158-66438159	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs190158132	chr7:66438283-66438284	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556329669	chr7:66438288-66438289	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374541938	chr7:66438306-66438307	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572825720	chr7:66438335-66438336	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200532327	chr7:66438426-66438427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535609057	chr7:66438456-66438457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113454159	chr7:66438500-66438501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144724903	chr7:66438526-66438527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539416094	chr7:66438601-66438602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552579025	chr7:66438617-66438618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541189987	chr7:66438620-66438621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558036157	chr7:66438621-66438622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577872770	chr7:66438625-66438626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12113509	chr7:66438654-66438655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543706513	chr7:66438660-66438661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563180026	chr7:66438669-66438670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367904814	chr7:66438673-66438674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201392600	chr7:66438724-66438725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572588792	chr7:66438732-66438733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528867422	chr7:66438741-66438742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113185988	chr7:66438755-66438756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200533252	chr7:66438763-66438764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371967551	chr7:66438778-66438779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374888010	chr7:66438781-66438782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs386714094	chr7:66438786-66438787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368141937	chr7:66438795-66438796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34644698	chr7:66438804-66438805	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs559371274	chr7:66438822-66438823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376354510	chr7:66438850-66438851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs386714095	chr7:66438852-66438853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373260451	chr7:66438857-66438858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201530898	chr7:66438882-66438883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199729296	chr7:66438888-66438889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182747206	chr7:66438895-66438896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200626452	chr7:66438921-66438922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551553130	chr7:66438928-66438929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571463184	chr7:66438934-66438935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10269977	chr7:66438944-66438945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530865267	chr7:66438945-66438946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113262124	chr7:66438947-66438948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550835844	chr7:66438952-66438953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112332831	chr7:66438973-66438974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75571515	chr7:66438987-66438988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10269991	chr7:66438989-66438990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111687742	chr7:66438992-66438993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535810786	chr7:66438996-66438997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555592768	chr7:66439002-66439003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77160186	chr7:66439009-66439010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187400478	chr7:66439035-66439036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD

Chromatin state (count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66420600-66459200	Weak transcription	Psoas Muscle	Psoas
2	chr7:66424400-66439600	Weak transcription	K562	blood
3	chr7:66426400-66453200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:66427000-66444800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:66427200-66438200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:66433200-66458600	Weak transcription	Right Atrium	heart
7	chr7:66435200-66438200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr7:66435200-66438800	Enhancers	Fetal Intestine Small	intestine
9	chr7:66436000-66440000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:66436000-66440200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr7:66437200-66438200	Flanking Active TSS	HepG2	liver
12	chr7:66437200-66438600	Enhancers	Fetal Intestine Large	intestine
13	chr7:66437200-66439000	Enhancers	Stomach Mucosa	stomach
14	chr7:66438000-66438200	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr7:66438000-66438400	Flanking Active TSS	Duodenum Mucosa	Duodenum
16	chr7:66438200-66438600	Enhancers	HepG2	liver
17	chr7:66438400-66439000	Enhancers	Duodenum Mucosa	Duodenum
18	chr7:66438800-66444800	Weak transcription	Fetal Intestine Small	intestine
19	chr7:66439000-66439600	Weak transcription	Stomach Mucosa	stomach
20	chr7:66439000-66445000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr7:66439600-66441200	Enhancers	K562	blood
22	chr7:66440000-66440400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr7:66440200-66440400	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr7:66440200-66440600	Enhancers	Dnd41	blood
25	chr7:66440400-66442800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:66442600-66444800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:66444800-66456800	Weak transcription	Stomach Mucosa	stomach
28	chr7:66445000-66445800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
29	chr7:66445400-66446000	ZNF genes & repeats	GM12878-XiMat	blood
30	chr7:66445800-66451600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr7:66445800-66452800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr7:66446000-66453200	Weak transcription	GM12878-XiMat	blood
33	chr7:66446200-66451800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:66446200-66453600	Weak transcription	Fetal Intestine Small	intestine
35	chr7:66446600-66459400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:66447000-66453000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:66448400-66450800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr7:66448400-66452200	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr7:66448800-66452000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr7:66448800-66452000	Weak transcription	Adipose Nuclei	Adipose
41	chr7:66449200-66449400	Enhancers	HepG2	liver
42	chr7:66449400-66451600	Weak transcription	Fetal Thymus	thymus
43	chr7:66449400-66451600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr7:66449400-66451800	Weak transcription	Primary B cells from peripheral blood	blood
45	chr7:66449400-66452200	Weak transcription	Colon Smooth Muscle	Colon
46	chr7:66449400-66453200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr7:66449400-66459200	Weak transcription	HepG2	liver
48	chr7:66449600-66451600	Weak transcription	HSMM	muscle
49	chr7:66449600-66451800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:66449600-66451800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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