Variant report

Variant	esv3386261
Chromosome Location	chr7:127991266-127993364
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:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:127992082..127994842-chr7:128029852..128032073,3	K562	blood:
2	chr7:127982362..127984093-chr7:127992558..127995177,2	MCF-7	breast:
3	chr7:127993211..127995208-chr7:128003186..128006029,2	K562	blood:
4	chr7:127991366..127994024-chr7:128043905..128046118,2	MCF-7	breast:
5	chr7:127992322..127995114-chr7:128014039..128015819,2	K562	blood:
6	chr7:127990878..127995208-chr7:127998293..128004686,6	K562	blood:
7	chr7:127989978..127992194-chr7:128000923..128002456,2	K562	blood:
8	chr7:127990359..127992194-chr7:128021875..128024379,2	MCF-7	breast:
9	chr7:127986655..127989567-chr7:127989980..127992814,3	K562	blood:
10	chr7:127913044..127915335-chr7:127992240..127993797,2	K562	blood:
11	chr7:127993298..127995820-chr7:128029600..128032073,2	K562	blood:
12	chr7:127989814..127992283-chr7:128027367..128029799,2	MCF-7	breast:
13	chr7:127992585..127993570-chr7:128027268..128027996,2	K562	blood:
14	chr7:127991141..127992839-chr7:127994705..127996789,2	K562	blood:
15	chr7:127982717..127985560-chr7:127989854..127991998,3	K562	blood:
16	chr7:127991021..127992566-chr7:128027560..128029110,2	MCF-7	breast:
17	chr7:127989735..127992397-chr7:128023905..128026447,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000106344	chromatin interactions
ENSG00000238750	chromatin interactions
ENSG00000106348	chromatin interactions
ENSG00000224940	chromatin interactions

Extended variants
information (count: 74 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577469431	chr7:127991327-127991328	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs541574687	chr7:127991330-127991331	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs559537456	chr7:127991340-127991341	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs145298449	chr7:127991440-127991441	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs34165256	chr7:127991490-127991491	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs541902137	chr7:127991571-127991572	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs563477339	chr7:127991602-127991603	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs34082547	chr7:127991614-127991615	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs373043864	chr7:127991670-127991671	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs530807269	chr7:127991678-127991679	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs552338648	chr7:127991680-127991681	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs565144222	chr7:127991715-127991716	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs532318746	chr7:127991731-127991732	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs547538114	chr7:127991753-127991754	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs565854233	chr7:127991756-127991757	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs148769759	chr7:127991855-127991856	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs548295951	chr7:127991869-127991870	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs569813034	chr7:127991873-127991874	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs537004624	chr7:127991882-127991883	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs558279481	chr7:127991926-127991927	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs571092037	chr7:127991935-127991936	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs535029813	chr7:127991936-127991937	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs142425872	chr7:127991965-127991966	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs13309008	chr7:127991967-127991968	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs553280441	chr7:127991989-127991990	Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs13309357	chr7:127992003-127992004	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs13309358	chr7:127992004-127992005	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs574678985	chr7:127992107-127992108	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542061624	chr7:127992140-127992141	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs557034031	chr7:127992142-127992143	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs575653936	chr7:127992178-127992179	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs546142939	chr7:127992234-127992235	Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs564343248	chr7:127992312-127992313	Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541759797	chr7:127992342-127992343	Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs528511964	chr7:127992345-127992346	Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs541314181	chr7:127992347-127992348	Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559726126	chr7:127992348-127992349	Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529910754	chr7:127992395-127992396	Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs1651945	chr7:127992437-127992438	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs569725348	chr7:127992468-127992469	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs530537093	chr7:127992530-127992531	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs552123372	chr7:127992542-127992543	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs13226601	chr7:127992572-127992573	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs570330844	chr7:127992574-127992575	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs534651389	chr7:127992584-127992585	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs553243997	chr7:127992585-127992586	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs185165197	chr7:127992607-127992608	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs376756635	chr7:127992609-127992610	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs374134322	chr7:127992631-127992632	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs557146395	chr7:127992651-127992652	Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127988200-127992200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr7:127990000-127991600	Weak transcription	Esophagus	oesophagus
3	chr7:127990400-127994400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:127991000-127991400	Bivalent Enhancer	Fetal Brain Female	brain
5	chr7:127991000-127991400	Bivalent Enhancer	Fetal Thymus	thymus
6	chr7:127991000-127991400	Enhancers	Right Ventricle	heart
7	chr7:127991000-127991600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
8	chr7:127991000-127991600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
9	chr7:127991000-127992800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr7:127991000-127993000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr7:127991200-127991400	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr7:127991200-127991400	Enhancers	Primary B cells from cord blood	blood
13	chr7:127991200-127991400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
14	chr7:127991200-127991400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
15	chr7:127991200-127991400	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
16	chr7:127991200-127991400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:127991200-127991400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr7:127991200-127991400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr7:127991200-127991400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
20	chr7:127991200-127991400	Bivalent Enhancer	Fetal Intestine Small	intestine
21	chr7:127991200-127991400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
22	chr7:127991200-127991400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
23	chr7:127991200-127991400	Bivalent Enhancer	Placenta	Placenta
24	chr7:127991200-127991600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
25	chr7:127991200-127991600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr7:127991200-127991600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:127991200-127991600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
28	chr7:127991200-127991800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr7:127991200-127992000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:127991200-127992000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
31	chr7:127991200-127992200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:127991200-127992800	Enhancers	Spleen	Spleen
33	chr7:127991200-127993000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:127991400-127991600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
35	chr7:127991400-127991600	Bivalent/Poised TSS	Primary T cells from cord blood	blood
36	chr7:127991400-127991600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr7:127991400-127991600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chr7:127991400-127991600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr7:127991400-127991600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr7:127991400-127991600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:127991400-127991600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
42	chr7:127991400-127991600	Bivalent/Poised TSS	Colonic Mucosa	Colon
43	chr7:127991400-127991600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
44	chr7:127991400-127991600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
45	chr7:127991400-127991600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
46	chr7:127991400-127991600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr7:127991400-127991600	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
48	chr7:127991400-127991600	Bivalent Enhancer	Lung	lung
49	chr7:127991400-127991600	Enhancers	Pancreas	Pancrea
50	chr7:127991400-127991600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle

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