Variant report

Variant	nsv884106
Chromosome Location	chr6:30775579-30787323
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:88)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:30780781..30783528-chr6:30792652..30795732,4	K562	blood:
2	chr6:30709799..30712568-chr6:30784877..30788022,4	K562	blood:
3	chr6:30765847..30772235-chr6:30775518..30781372,10	K562	blood:
4	chr6:30735402..30739247-chr6:30785239..30791444,10	MCF-7	breast:
5	chr6:30696761..30700438-chr6:30779538..30781456,3	K562	blood:
6	chr6:30698701..30700492-chr6:30786748..30789246,2	MCF-7	breast:
7	chr6:30760063..30761714-chr6:30779972..30782451,2	K562	blood:
8	chr6:30786581..30788295-chr6:30794168..30796085,2	MCF-7	breast:
9	chr6:30756080..30757892-chr6:30785304..30787449,2	MCF-7	breast:
10	chr6:30781901..30784193-chr6:30851242..30852873,2	K562	blood:
11	chr6:30703055..30723531-chr6:30783853..30800217,151	MCF-7	breast:
12	chr6:30776031..30777609-chr6:30851377..30854033,2	MCF-7	breast:
13	chr11:65196773..65198444-chr6:30776938..30778941,2	MCF-7	breast:
14	chr6:30742999..30744721-chr6:30782116..30783840,2	MCF-7	breast:
15	chr6:30766009..30775294-chr6:30775700..30782710,15	MCF-7	breast:
16	chr6:30777633..30780399-chr6:30780437..30782571,2	MCF-7	breast:
17	chr6:30775890..30781762-chr6:30785090..30789723,9	MCF-7	breast:
18	chr6:30745917..30748118-chr6:30776110..30778177,2	K562	blood:
19	chr6:30775890..30781762-chr6:30785090..30789723,9	MCF-7	breast:
20	chr6:30786686..30788380-chr6:30859735..30862378,2	MCF-7	breast:
21	chr6:30757568..30759864-chr6:30782020..30783949,2	K562	blood:
22	chr6:30583858..30586014-chr6:30781154..30783214,2	K562	blood:
23	chr6:30779954..30784896-chr6:30785156..30789787,6	K562	blood:
24	chr6:30687859..30690544-chr6:30777327..30780060,3	MCF-7	breast:
25	chr6:30782149..30783848-chr6:30788583..30790085,2	MCF-7	breast:
26	chr6:30739130..30742242-chr6:30780166..30782431,3	K562	blood:
27	chr6:30777633..30780399-chr6:30780437..30782571,2	MCF-7	breast:
28	chr6:30648527..30651008-chr6:30780942..30782992,2	K562	blood:
29	chr6:30582861..30585140-chr6:30778176..30780567,2	MCF-7	breast:
30	chr6:30456417..30458874-chr6:30776787..30780179,3	K562	blood:
31	chr6:30655802..30657936-chr6:30780184..30782576,2	K562	blood:
32	chr6:30762133..30768787-chr6:30785989..30790050,8	MCF-7	breast:
33	chr6:30752526..30755713-chr6:30784163..30787914,3	MCF-7	breast:
34	chr6:30781732..30783856-chr6:30842291..30844070,2	K562	blood:
35	chr6:30716968..30722090-chr6:30774929..30783584,12	MCF-7	breast:
36	chr6:30780089..30782522-chr6:30839223..30841388,2	K562	blood:
37	chr6:30747572..30751987-chr6:30785552..30789586,6	MCF-7	breast:
38	chr6:30778242..30780250-chr6:30790501..30792302,2	K562	blood:
39	chr6:30785152..30790346-chr6:30842867..30847278,6	K562	blood:
40	chr6:30786994..30789878-chr6:30922347..30924332,2	K562	blood:
41	chr6:30774980..30776626-chr6:30874268..30876339,2	K562	blood:
42	chr6:30784948..30788264-chr6:30874888..30877242,3	MCF-7	breast:
43	chr6:30703666..30722133-chr6:30776009..30801352,184	MCF-7	breast:
44	chr6:30782136..30784193-chr6:30786260..30788074,2	MCF-7	breast:
45	chr6:30723722..30725318-chr6:30780845..30782479,3	MCF-7	breast:
46	chr6:30778063..30780102-chr8:113652986..113654698,2	MCF-7	breast:
47	chr6:30776586..30778152-chr6:30852423..30854112,2	MCF-7	breast:
48	chr6:30744501..30746062-chr6:30781081..30782628,2	K562	blood:
49	chr6:30777372..30779783-chr6:30849270..30851072,2	K562	blood:
50	chr6:30710566..30711266-chr6:30785718..30786636,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IER3-5	chr6:30780643-30782549	ENSG00000214894

No data

Variant related genes	Relation type
ENSG00000204569	chromatin interactions
ENSG00000204580	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000196230	chromatin interactions
ENSG00000138346	chromatin interactions
ENSG00000137411	chromatin interactions
ENSG00000204576	chromatin interactions
ENSG00000263608	chromatin interactions
ENSG00000204592	chromatin interactions
ENSG00000272540	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000237775	chromatin interactions
ENSG00000264731	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000228022	chromatin interactions
ENSG00000233529	chromatin interactions
ENSG00000204590	chromatin interactions
ENSG00000201988	chromatin interactions
ENSG00000213780	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000137331	chromatin interactions

Extended variants
information (count: 597 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9391634	chr6:30775579-30775580	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs28890780	chr6:30775590-30775591	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs538612892	chr6:30775599-30775600	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs147400439	chr6:30775645-30775646	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs28877339	chr6:30775685-30775686	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557630186	chr6:30775693-30775694	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs574282612	chr6:30775713-30775714	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs9378110	chr6:30775733-30775734	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs559783758	chr6:30775800-30775801	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs9391635	chr6:30775805-30775806	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs139795304	chr6:30775837-30775838	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs565084196	chr6:30775840-30775841	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs35333913	chr6:30775911-30775912	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs9295920	chr6:30775941-30775942	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs564175194	chr6:30776032-30776033	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs181674220	chr6:30776076-30776077	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs185957558	chr6:30776109-30776110	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs529816576	chr6:30776127-30776128	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs546411558	chr6:30776131-30776132	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs35476622	chr6:30776134-30776135	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs9281052	chr6:30776144-30776145	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs13197382	chr6:30776145-30776146	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs190332114	chr6:30776149-30776150	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs9404970	chr6:30776174-30776175	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs386698803	chr6:30776195-30776196	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs9391692	chr6:30776197-30776198	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs114514827	chr6:30776225-30776226	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs182495394	chr6:30776228-30776229	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs9404972	chr6:30776229-30776230	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs9404973	chr6:30776232-30776233	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs536870475	chr6:30776239-30776240	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs112151218	chr6:30776259-30776260	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs573287460	chr6:30776265-30776266	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs565198131	chr6:30776292-30776293	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs201606647	chr6:30776302-30776303	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs369612662	chr6:30776303-30776304	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs186819504	chr6:30776318-30776319	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs564976938	chr6:30776371-30776372	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs575229045	chr6:30776382-30776383	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs9391693	chr6:30776393-30776394	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs371589119	chr6:30776435-30776436	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs190737547	chr6:30776450-30776451	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs116249613	chr6:30776457-30776458	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs529615886	chr6:30776470-30776471	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs184230197	chr6:30776478-30776479	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs9404974	chr6:30776483-30776484	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs549396403	chr6:30776563-30776564	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs145785213	chr6:30776601-30776602	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs112882372	chr6:30776617-30776618	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs12200562	chr6:30776621-30776622	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30761600-30781000	Weak transcription	Small Intestine	intestine
2	chr6:30767200-30781200	Weak transcription	Gastric	stomach
3	chr6:30771200-30777400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:30772200-30777200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr6:30772400-30777000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr6:30772600-30776600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr6:30772600-30777600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr6:30772600-30778000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr6:30772600-30778400	Weak transcription	Fetal Thymus	thymus
10	chr6:30772800-30776000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr6:30772800-30776400	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr6:30772800-30778200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr6:30773000-30776600	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr6:30773000-30778600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:30773200-30775800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr6:30773400-30778200	Weak transcription	Primary T cells from cord blood	blood
17	chr6:30773800-30776400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr6:30774600-30775600	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr6:30774600-30777200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:30774600-30777200	Weak transcription	K562	blood
21	chr6:30774800-30779800	Weak transcription	HepG2	liver
22	chr6:30775000-30778400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:30775000-30778600	Weak transcription	Placenta	Placenta
24	chr6:30775600-30776400	Weak transcription	Primary B cells from cord blood	blood
25	chr6:30775600-30777800	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr6:30775800-30776600	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr6:30776000-30776200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:30776000-30776600	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr6:30776200-30777200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:30776200-30779000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr6:30776400-30776600	Enhancers	Primary B cells from cord blood	blood
32	chr6:30776400-30779000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr6:30776400-30783200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr6:30776400-30783400	Enhancers	Primary T cells fromperipheralblood	blood
35	chr6:30776600-30776800	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr6:30776600-30778000	Weak transcription	Primary B cells from cord blood	blood
37	chr6:30776600-30779800	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr6:30776600-30780000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr6:30776600-30783400	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr6:30776800-30777200	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr6:30776800-30779000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr6:30777000-30780400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:30777200-30777400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:30777200-30777400	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr6:30777200-30777400	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr6:30777200-30777600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr6:30777200-30777800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr6:30777200-30778200	Enhancers	GM12878-XiMat	blood
49	chr6:30777200-30779000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr6:30777200-30779000	Enhancers	HUES48 Cell Line	embryonic stem cell

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