Variant report

Variant	nsv884107
Chromosome Location	chr6:30776483-30787323
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:87)
LncRNA
region (count:1)
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	chr6:30757568..30759864-chr6:30782020..30783949,2	K562	blood:
2	chr6:30698701..30700492-chr6:30786748..30789246,2	MCF-7	breast:
3	chr6:30749778..30751326-chr6:30778307..30780023,3	MCF-7	breast:
4	chr6:30772437..30774546-chr6:30775757..30777964,2	MCF-7	breast:
5	chr6:30774980..30776626-chr6:30874268..30876339,2	K562	blood:
6	chr6:30709799..30712568-chr6:30784877..30788022,4	K562	blood:
7	chr6:30703055..30723531-chr6:30783853..30800217,151	MCF-7	breast:
8	chr6:30522929..30524669-chr6:30781781..30783555,2	K562	blood:
9	chr6:30786581..30788295-chr6:30794168..30796085,2	MCF-7	breast:
10	chr6:30583858..30586014-chr6:30781154..30783214,2	K562	blood:
11	chr6:30775890..30781762-chr6:30785090..30789723,9	MCF-7	breast:
12	chr6:30782254..30784176-chr6:30785008..30786775,3	K562	blood:
13	chr6:30760063..30761714-chr6:30779972..30782451,2	K562	blood:
14	chr6:30781732..30783856-chr6:30842291..30844070,2	K562	blood:
15	chr6:30745917..30748118-chr6:30776110..30778177,2	K562	blood:
16	chr6:30456417..30458874-chr6:30776787..30780179,3	K562	blood:
17	chr6:30742999..30744721-chr6:30782116..30783840,2	MCF-7	breast:
18	chr6:30687466..30692169-chr6:30775918..30784078,7	K562	blood:
19	chr6:30716968..30722090-chr6:30774929..30783584,12	MCF-7	breast:
20	chr6:30782254..30784176-chr6:30785008..30786775,3	K562	blood:
21	chr6:30781714..30783791-chr6:30982862..30984438,2	K562	blood:
22	chr6:30720149..30720893-chr6:30781568..30782338,2	MCF-7	breast:
23	chr6:30784327..30791562-chr6:30848580..30853873,26	MCF-7	breast:
24	chr6:30782463..30785356-chr6:30842296..30844598,2	K562	blood:
25	chr6:30780643..30783504-chr6:30803282..30805852,2	K562	blood:
26	chr6:30779954..30784896-chr6:30785156..30789787,6	K562	blood:
27	chr6:30767146..30768720-chr6:30776918..30779090,2	MCF-7	breast:
28	chr6:30784917..30788265-chr6:30788350..30790459,3	K562	blood:
29	chr6:30780089..30782522-chr6:30839223..30841388,2	K562	blood:
30	chr10:70231407..70232217-chr6:30782771..30783463,2	Hela-S3	cervix:
31	chr6:30760214..30763491-chr6:30779624..30782451,3	K562	blood:
32	chr6:30777372..30779783-chr6:30849270..30851072,2	K562	blood:
33	chr6:30777633..30780399-chr6:30780437..30782571,2	MCF-7	breast:
34	chr6:30780598..30803497-chr6:30842531..30855110,80	MCF-7	breast:
35	chr6:30762133..30768787-chr6:30785989..30790050,8	MCF-7	breast:
36	chr6:30753093..30755671-chr6:30782246..30783854,2	K562	blood:
37	chr6:30778242..30780250-chr6:30790501..30792302,2	K562	blood:
38	chr6:30765847..30772235-chr6:30775518..30781372,10	K562	blood:
39	chr6:30703666..30722133-chr6:30776009..30801352,184	MCF-7	breast:
40	chr6:30766009..30775294-chr6:30775700..30782710,15	MCF-7	breast:
41	chr6:30786994..30789878-chr6:30922347..30924332,2	K562	blood:
42	chr6:30693275..30696224-chr6:30778287..30780136,2	K562	blood:
43	chr6:30756080..30757892-chr6:30785304..30787449,2	MCF-7	breast:
44	chr6:30782136..30784193-chr6:30786260..30788074,2	MCF-7	breast:
45	chr6:30687402..30688966-chr6:30782150..30783653,2	K562	blood:
46	chr6:30785152..30790346-chr6:30842867..30847278,6	K562	blood:
47	chr6:30648527..30651008-chr6:30780942..30782992,2	K562	blood:
48	chr6:30782136..30784193-chr6:30786260..30788074,2	MCF-7	breast:
49	chr6:30781901..30784193-chr6:30851242..30852873,2	K562	blood:
50	chr6:30779954..30784896-chr6:30785156..30789787,6	K562	blood:

(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
ENSG00000222894	chromatin interactions
ENSG00000201988	chromatin interactions
ENSG00000272540	chromatin interactions
ENSG00000138346	chromatin interactions
ENSG00000196230	chromatin interactions
ENSG00000204580	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000263608	chromatin interactions
ENSG00000204590	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000228022	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000233529	chromatin interactions
ENSG00000264731	chromatin interactions
ENSG00000237775	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000204576	chromatin interactions
ENSG00000204592	chromatin interactions
ENSG00000137411	chromatin interactions
ENSG00000213780	chromatin interactions

Extended variants
information (count: 552 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:552 , 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	rs9404974	chr6:30776483-30776484	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549396403	chr6:30776563-30776564	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs145785213	chr6:30776601-30776602	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs112882372	chr6:30776617-30776618	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs12200562	chr6:30776621-30776622	Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs148531217	chr6:30776677-30776678	Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs6934949	chr6:30776708-30776709	Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs116767578	chr6:30776713-30776714	Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs553537865	chr6:30776722-30776723	Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs9391694	chr6:30776725-30776726	Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs539167967	chr6:30776772-30776773	Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs144440222	chr6:30776793-30776794	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs9295921	chr6:30776802-30776803	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544213153	chr6:30776814-30776815	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs117952206	chr6:30776828-30776829	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs146600641	chr6:30776846-30776847	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs530629683	chr6:30776857-30776858	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs9295922	chr6:30776858-30776859	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12200829	chr6:30776896-30776897	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs555322521	chr6:30776959-30776960	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs12214232	chr6:30776960-30776961	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs562588171	chr6:30776971-30776972	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs141453131	chr6:30777027-30777028	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs200562733	chr6:30777049-30777050	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs369038540	chr6:30777068-30777069	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs61218470	chr6:30777070-30777071	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs9380193	chr6:30777149-30777150	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs530461957	chr6:30777197-30777198	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs9368641	chr6:30777237-30777238	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs9380194	chr6:30777258-30777259	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs12214398	chr6:30777261-30777262	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs558691104	chr6:30777278-30777279	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs199821434	chr6:30777286-30777287	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs12208098	chr6:30777321-30777322	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs9380195	chr6:30777327-30777328	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs554584706	chr6:30777331-30777332	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs145145614	chr6:30777344-30777345	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs146426173	chr6:30777366-30777367	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs553767312	chr6:30777422-30777423	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs376556920	chr6:30777431-30777432	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs577035046	chr6:30777458-30777459	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs188720257	chr6:30777484-30777485	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs1264361	chr6:30777498-30777499	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs374025349	chr6:30777501-30777502	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs568951256	chr6:30777528-30777529	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs531445759	chr6:30777588-30777589	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs9394017	chr6:30777604-30777605	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs561767274	chr6:30777616-30777617	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs140657469	chr6:30777639-30777640	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs193221865	chr6:30777643-30777644	Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

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:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr6:30772800-30778200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr6:30773000-30776600	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr6:30773000-30778600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:30773400-30778200	Weak transcription	Primary T cells from cord blood	blood
14	chr6:30774600-30777200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:30774600-30777200	Weak transcription	K562	blood
16	chr6:30774800-30779800	Weak transcription	HepG2	liver
17	chr6:30775000-30778400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:30775000-30778600	Weak transcription	Placenta	Placenta
19	chr6:30775600-30777800	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr6:30775800-30776600	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr6:30776000-30776600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr6:30776200-30777200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:30776200-30779000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr6:30776400-30776600	Enhancers	Primary B cells from cord blood	blood
25	chr6:30776400-30779000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr6:30776400-30783200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr6:30776400-30783400	Enhancers	Primary T cells fromperipheralblood	blood
28	chr6:30776600-30776800	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr6:30776600-30778000	Weak transcription	Primary B cells from cord blood	blood
30	chr6:30776600-30779800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr6:30776600-30780000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr6:30776600-30783400	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr6:30776800-30777200	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr6:30776800-30779000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr6:30777000-30780400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr6:30777200-30777400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:30777200-30777400	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr6:30777200-30777400	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr6:30777200-30777600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr6:30777200-30777800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr6:30777200-30778200	Enhancers	GM12878-XiMat	blood
42	chr6:30777200-30779000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr6:30777200-30779000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr6:30777200-30779000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr6:30777200-30779200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr6:30777200-30781000	Enhancers	K562	blood
47	chr6:30777200-30783200	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr6:30777400-30777600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr6:30777400-30777600	Enhancers	Colonic Mucosa	Colon
50	chr6:30777400-30778000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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