Variant report

Variant	nsv538654
Chromosome Location	chr7:2750418-2781716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:87)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr7:2761837..2763894-chr7:2912353..2913943,2	MCF-7	breast:
2	chr7:2760677..2762584-chr7:2771267..2773265,2	MCF-7	breast:
3	chr7:2559563..2562447-chr7:2751548..2753355,2	MCF-7	breast:
4	chr18:33161346..33162077-chr7:2758154..2758655,2	HCT-116	colon:
5	chr7:2758294..2760218-chr7:2772871..2774400,2	MCF-7	breast:
6	chr7:2756357..2758230-chr7:2913588..2915207,2	K562	blood:
7	chr7:2749256..2751916-chr7:2756659..2758882,3	K562	blood:
8	chr7:2710494..2711221-chr7:2758292..2759192,2	MCF-7	breast:
9	chr7:2727234..2729043-chr7:2757444..2760192,2	MCF-7	breast:
10	chr7:2769685..2774579-chr7:2777594..2780364,4	K562	blood:
11	chr7:2760749..2763045-chr7:2764793..2766522,2	K562	blood:
12	chr7:2727165..2732362-chr7:2746794..2750552,7	MCF-7	breast:
13	chr10:112773361..112773861-chr7:2758450..2759306,2	MCF-7	breast:
14	chr7:2710355..2711188-chr7:2758257..2758996,5	MCF-7	breast:
15	chr7:2763542..2765998-chr7:2913273..2914846,2	MCF-7	breast:
16	chr7:2753727..2755444-chr7:2914666..2916537,2	MCF-7	breast:
17	chr7:2757202..2759716-chr7:2762662..2764833,2	K562	blood:
18	chr7:2751886..2754183-chr7:2882773..2885002,2	K562	blood:
19	chr7:2748815..2750659-chr7:2753960..2755494,2	MCF-7	breast:
20	chr7:2758129..2761976-chr7:2763173..2766287,3	MCF-7	breast:
21	chr12:58138577..58140226-chr7:2752258..2753758,2	MCF-7	breast:
22	chr7:2760749..2763045-chr7:2764793..2766522,2	K562	blood:
23	chr7:2777523..2779993-chr7:2788582..2791308,2	MCF-7	breast:
24	chr7:2756029..2757761-chr7:2771814..2773662,2	MCF-7	breast:
25	chr7:2747802..2752072-chr7:2752381..2756617,8	K562	blood:
26	chr7:2770258..2772875-chr7:2776418..2779322,2	MCF-7	breast:
27	chr7:2768256..2774537-chr7:2775031..2780281,7	K562	blood:
28	chr7:2776568..2779036-chr7:2798696..2800622,2	MCF-7	breast:
29	chr7:2770824..2773530-chr7:2796217..2798133,2	K562	blood:
30	chr7:2729178..2731029-chr7:2755632..2757456,2	MCF-7	breast:
31	chr7:2769685..2774579-chr7:2777594..2780364,4	K562	blood:
32	chr7:2755108..2758694-chr7:2796336..2799311,5	K562	blood:
33	chr7:2734820..2736762-chr7:2751903..2754029,2	MCF-7	breast:
34	chr7:2758216..2760821-chr7:2762447..2764162,2	K562	blood:
35	chr7:2775731..2778086-chr7:2883079..2885342,2	MCF-7	breast:
36	chr7:2757306..2759067-chr7:2759260..2762192,2	K562	blood:
37	chr7:2650921..2653062-chr7:2755839..2758657,2	MCF-7	breast:
38	chr7:2770258..2772875-chr7:2776418..2779322,2	MCF-7	breast:
39	chr7:2651950..2654587-chr7:2749011..2751356,2	K562	blood:
40	chr7:2755108..2759929-chr7:2796424..2799629,5	K562	blood:
41	chr7:2726976..2732306-chr7:2751812..2755124,4	MCF-7	breast:
42	chr7:2749256..2751916-chr7:2756659..2758882,3	K562	blood:
43	chr7:2727069..2729394-chr7:2748940..2750951,2	MCF-7	breast:
44	chr7:2758216..2760821-chr7:2762447..2764162,2	K562	blood:
45	chr7:2393560..2395423-chr7:2757362..2759137,2	K562	blood:
46	chr7:2767711..2769889-chr7:2772615..2775037,2	MCF-7	breast:
47	chr7:2749388..2752316-chr7:2798126..2801115,2	K562	blood:
48	chr7:2737260..2740261-chr7:2747906..2751083,3	K562	blood:
49	chr7:2768256..2774537-chr7:2775031..2780281,7	K562	blood:
50	chr7:2760677..2762584-chr7:2771267..2773265,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNA12-1	chr7:2763099-2764726	XLOC_006336
2	lnc-BRAT1-3	chr7:2768098-2768523	NONHSAT118825
3	lnc-TTYH3-2	chr7:2762818-2764609	NONHSAT118823
4	lnc-GNA12-2	chr7:2757467-2760269	XLOC_006335
5	lnc-GNA12-2	chr7:2762138-2762622	XLOC_006335
6	lnc-GNA12-1	chr7:2761466-2761772	XLOC_006336

No data

Variant related genes	Relation type
ENSG00000174945	chromatin interactions
ENSG00000106263	chromatin interactions
ENSG00000106266	chromatin interactions
ENSG00000135452	chromatin interactions
ENSG00000106009	chromatin interactions
ENSG00000146535	chromatin interactions
ENSG00000141429	chromatin interactions

Extended variants
information (count: 2104 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2104 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148303973	chr7:2750418-2750419	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs374650372	chr7:2750419-2750420	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531936855	chr7:2750437-2750438	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs75865347	chr7:2750449-2750450	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs61128220	chr7:2750450-2750451	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs532757878	chr7:2750454-2750455	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369344846	chr7:2750487-2750488	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs540259117	chr7:2750506-2750507	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559970404	chr7:2750524-2750525	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs184511854	chr7:2750527-2750528	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs549188872	chr7:2750541-2750542	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs569030875	chr7:2750556-2750557	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs531535913	chr7:2750576-2750577	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs116779033	chr7:2750591-2750592	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189224123	chr7:2750632-2750633	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs538146967	chr7:2750633-2750634	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs181197794	chr7:2750679-2750680	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529782215	chr7:2750693-2750694	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs567698981	chr7:2750702-2750703	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs553382132	chr7:2750742-2750743	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370057449	chr7:2750744-2750745	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566845615	chr7:2750745-2750746	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs374755772	chr7:2750753-2750754	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs798567	chr7:2750763-2750764	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
25	rs4721982	chr7:2750768-2750769	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs798566	chr7:2750769-2750770	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs558152738	chr7:2750776-2750777	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs578218205	chr7:2750834-2750835	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs539844799	chr7:2750851-2750852	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560132772	chr7:2750856-2750857	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs10252130	chr7:2750918-2750919	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs542696158	chr7:2750922-2750923	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs562591969	chr7:2750929-2750930	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs531496733	chr7:2750961-2750962	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551584142	chr7:2750977-2750978	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs565033490	chr7:2750983-2750984	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs184283007	chr7:2751021-2751022	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs547386747	chr7:2751031-2751032	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7803527	chr7:2751040-2751041	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs189350898	chr7:2751050-2751051	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561329892	chr7:2751063-2751064	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549033984	chr7:2751113-2751114	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552459504	chr7:2751144-2751145	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569045215	chr7:2751146-2751147	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538034335	chr7:2751196-2751197	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558376774	chr7:2751208-2751209	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141556474	chr7:2751213-2751214	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571671781	chr7:2751223-2751224	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534463014	chr7:2751247-2751248	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114014577	chr7:2751255-2751256	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute myeloid leukemia	19651601	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Cancer	17160897	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17142309	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1607 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:2741800-2753200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr7:2742000-2751800	Weak transcription	NHLF	lung
3	chr7:2742200-2765600	Weak transcription	HSMM	muscle
4	chr7:2746000-2750800	Enhancers	Placenta	Placenta
5	chr7:2746600-2753000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr7:2747800-2753800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:2748400-2751000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:2748400-2751200	Flanking Active TSS	GM12878-XiMat	blood
9	chr7:2748400-2751400	Enhancers	Primary hematopoietic stem cells	blood
10	chr7:2748400-2752000	Enhancers	Primary B cells from cord blood	blood
11	chr7:2748600-2751200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr7:2748600-2751400	Bivalent Enhancer	Fetal Thymus	thymus
13	chr7:2748800-2750600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:2748800-2755400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:2749000-2750800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
16	chr7:2749000-2750800	Flanking Active TSS	Primary B cells from peripheral blood	blood
17	chr7:2749000-2753400	Enhancers	Dnd41	blood
18	chr7:2749000-2760800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr7:2749200-2750800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
20	chr7:2749200-2751000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:2749200-2751200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
22	chr7:2749400-2751000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
23	chr7:2749400-2754800	Weak transcription	Fetal Brain Female	brain
24	chr7:2749400-2755600	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr7:2749400-2770600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr7:2749600-2750600	Weak transcription	Esophagus	oesophagus
27	chr7:2749600-2750800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:2749600-2751800	Weak transcription	Left Ventricle	heart
29	chr7:2749600-2752200	Weak transcription	Ovary	ovary
30	chr7:2749800-2751400	Enhancers	Primary T cells from cord blood	blood
31	chr7:2749800-2751400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr7:2749800-2751800	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr7:2749800-2751800	Weak transcription	Right Ventricle	heart
34	chr7:2749800-2752000	Weak transcription	Right Atrium	heart
35	chr7:2749800-2752200	Weak transcription	Fetal Lung	lung
36	chr7:2749800-2752800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr7:2749800-2753000	Weak transcription	Stomach Smooth Muscle	stomach
38	chr7:2749800-2753000	Weak transcription	K562	blood
39	chr7:2749800-2753400	Weak transcription	Pancreas	Pancrea
40	chr7:2749800-2757600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr7:2749800-2758000	Weak transcription	Brain Anterior Caudate	brain
42	chr7:2749800-2759800	Weak transcription	HMEC	breast
43	chr7:2749800-2770800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:2750000-2750600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr7:2750000-2750600	Weak transcription	Brain Germinal Matrix	brain
46	chr7:2750000-2750600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr7:2750000-2750600	Weak transcription	Gastric	stomach
48	chr7:2750000-2750800	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr7:2750000-2751000	Bivalent Enhancer	Colonic Mucosa	Colon
50	chr7:2750000-2751000	Weak transcription	Fetal Heart	heart

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