Variant report

Variant	esv3436059
Chromosome Location	chr6:36986674-36990872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:495)
CpG islands
(count:0)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:36989395-36989810	K562	blood:	n/a	n/a
2	ARID3A	chr6:36986002-36986764	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:36985997-36986807	K562	blood:	n/a	n/a
4	ATF3	chr6:36989521-36989856	K562	blood:	n/a	n/a
5	BACH1	chr6:36989735-36989791	K562	blood:	n/a	n/a
6	BCLAF1	chr6:36985916-36986759	GM12878	blood:	n/a	n/a
7	BCLAF1	chr6:36985945-36986799	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:36985940-36986736	K562	blood:	n/a	n/a
9	BHLHE40	chr6:36989486-36989851	K562	blood:	n/a	n/a
10	BRCA1	chr6:36989574-36989696	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr6:36985945-36986764	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr6:36989404-36989950	K562	blood:	n/a	n/a
13	CBX3	chr6:36985856-36986788	K562	blood:	n/a	n/a
14	CBX3	chr6:36989536-36989847	K562	blood:	n/a	n/a
15	CCNT2	chr6:36989580-36989901	K562	blood:	n/a	n/a
16	CEBPB	chr6:36986848-36987319	MCF-7	breast:	n/a	n/a
17	CEBPB	chr6:36989633-36989674	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr6:36989483-36989826	K562	blood:	n/a	n/a
19	CHD2	chr6:36989637-36989685	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr6:36989540-36989690	HAc	cerebellar:	n/a	n/a
21	CTCF	chr6:36989486-36989731	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr6:36985982-36986737	HUVEC	blood vessel:	n/a	chr6:36986115-36986133
23	CTCF	chr6:36989434-36989840	K562	blood:	n/a	n/a
24	CTCF	chr6:36985978-36986737	GM12878	blood:	n/a	chr6:36986115-36986133
25	CTCF	chr6:36985245-36987544	SK-N-SH	brain:	n/a	chr6:36986115-36986133
26	CTCF	chr6:36987120-36987270	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr6:36987080-36987230	HEK293	kidney:	n/a	n/a
28	CTCF	chr6:36989520-36989670	GM12865	blood:	n/a	n/a
29	CTCF	chr6:36985914-36986866	K562	blood:	n/a	chr6:36986115-36986133
30	CTCF	chr6:36986540-36986690	HepG2	liver:	n/a	n/a
31	CTCF	chr6:36989335-36990015	A549	lung:	n/a	n/a
32	CTCF	chr6:36989493-36989758	K562	blood:	n/a	n/a
33	CTCF	chr6:36985980-36986696	NHEK	skin:	n/a	chr6:36986115-36986133
34	CTCF	chr6:36989560-36989710	AG04450	lung:	n/a	n/a
35	CTCF	chr6:36989138-36990083	SK-N-SH	brain:	n/a	n/a
36	CTCF	chr6:36989529-36989726	GM12891	blood:	n/a	n/a
37	CTCF	chr6:36988220-36988370	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:36989580-36989730	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr6:36989500-36989650	GM12864	blood:	n/a	n/a
40	CTCF	chr6:36989600-36989750	HCM	heart:	n/a	n/a
41	CTCF	chr6:36986780-36986930	BE2_C	brain:	n/a	n/a
42	CTCF	chr6:36989580-36989730	GM12872	blood:	n/a	n/a
43	CTCF	chr6:36985892-36986827	A549	lung:	n/a	chr6:36986115-36986133
44	CTCF	chr6:36985990-36986709	GM13977	blood:	n/a	chr6:36986115-36986133
45	CTCF	chr6:36989528-36989720	Fibrobl	skin:	n/a	n/a
46	CTCF	chr6:36989512-36989745	NHEK	skin:	n/a	n/a
47	CTCF	chr6:36985983-36986715	Medullo	brain:	n/a	chr6:36986115-36986133
48	CTCF	chr6:36985865-36986818	T-47D	breast:	n/a	chr6:36986115-36986133
49	CTCF	chr6:36988280-36988430	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr6:36989539-36989739	GM10248	blood:	n/a	n/a

No data

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:36985845..36988567-chr6:37138212..37140631,3	K562	blood:
2	chr6:36886183..36886832-chr6:36986137..36986795,2	MCF-7	breast:
3	chr6:36947258..36950041-chr6:36986048..36987573,2	MCF-7	breast:
4	chr6:36951647..36954567-chr6:36984468..36987638,6	K562	blood:
5	chr6:36980695..36984451-chr6:36985282..36988423,5	K562	blood:
6	chr6:36989372..36991434-chr6:37069040..37071610,2	MCF-7	breast:
7	chr6:36985689..36987067-chr6:37174835..37176439,10	MCF-7	breast:
8	chr6:36989418..36991271-chr6:36992892..36995334,2	K562	blood:
9	chr6:36990423..36992455-chr6:37172095..37173787,2	K562	blood:
10	chr6:36986126..36987117-chr6:37176530..37177578,3	MCF-7	breast:
11	chr6:36989691..36991271-chr6:36992892..36995062,3	K562	blood:
12	chr6:36831717..36834035-chr6:36985083..36987828,2	K562	blood:
13	chr6:36985833..36987427-chr6:37139677..37140666,12	MCF-7	breast:
14	chr6:36852005..36855458-chr6:36984429..36987560,3	K562	blood:
15	chr6:36987000..36988996-chr6:36992167..36994325,2	MCF-7	breast:
16	chr6:36986189..36986703-chr6:36997156..36997970,2	K562	blood:
17	chr6:36990515..36993191-chr6:37140306..37142032,2	K562	blood:
18	chr6:36985701..36987115-chr6:37175477..37176997,13	K562	blood:
19	chr6:36986109..36986997-chr6:37018972..37019835,3	MCF-7	breast:
20	chr6:36987509..36988444-chr6:37177937..37178601,3	K562	blood:
21	chr6:36990365..36993008-chr6:37173056..37174910,2	MCF-7	breast:
22	chr6:36990308..36994435-chr6:37135955..37142463,7	MCF-7	breast:
23	chr6:36984736..36987348-chr6:37138212..37139729,2	K562	blood:
24	chr6:36985952..36987180-chr6:37139557..37141095,24	K562	blood:
25	chr6:36989705..36991355-chr6:37177906..37180017,2	K562	blood:
26	chr6:36989098..36990112-chr6:37139646..37140588,5	K562	blood:
27	chr6:36985904..36987716-chr6:37141908..37143451,2	MCF-7	breast:
28	chr6:36986077..36986711-chr6:37180681..37181810,4	K562	blood:
29	chr6:36928588..36930558-chr6:36986253..36988587,2	K562	blood:
30	chr6:36986055..36987477-chr6:37177799..37178902,22	MCF-7	breast:
31	chr6:36985158..36987310-chr6:37189028..37190861,2	K562	blood:
32	chr6:36733415..36734583-chr6:36985207..36986995,7	MCF-7	breast:
33	chr6:36986111..36987939-chr6:37176127..37178450,2	MCF-7	breast:
34	chr6:36989173..36991551-chr6:37137394..37139647,3	K562	blood:
35	chr6:36851998..36854194-chr6:36984664..36987550,2	K562	blood:
36	chr6:36733549..36734625-chr6:36985573..36986688,19	K562	blood:
37	chr6:36985829..36988521-chr6:36988646..36990558,2	K562	blood:
38	chr6:36986227..36987023-chr6:37179191..37179864,2	MCF-7	breast:
39	chr6:36986123..36987013-chr6:36995872..36996986,3	K562	blood:
40	chr6:36990051..36995346-chr6:37136390..37139647,6	K562	blood:
41	chr6:36944786..36946944-chr6:36988246..36989759,2	MCF-7	breast:
42	chr6:36926516..36929397-chr6:36985217..36986948,2	K562	blood:
43	chr6:36990146..36994003-chr6:37137207..37141161,5	MCF-7	breast:
44	chr6:36989570..36992539-chr6:37178142..37179821,2	MCF-7	breast:
45	chr6:36990791..36991393-chr6:37175987..37176512,2	K562	blood:
46	chr6:36984774..36987733-chr6:36993476..36997065,5	K562	blood:
47	chr6:36985644..36987482-chr6:37177455..37178899,11	MCF-7	breast:
48	chr6:36989505..36991415-chr6:36995722..36997546,2	K562	blood:
49	chr6:36985713..36987315-chr6:37177177..37178923,41	K562	blood:
50	chr6:36952434..36955977-chr6:36983476..36987276,5	MCF-7	breast:

No data

Variant related genes	Relation type
FGD2	TF binding region
ENSG00000112130	chromatin interactions
ENSG00000146192	chromatin interactions
ENSG00000198663	chromatin interactions
ENSG00000137193	chromatin interactions
ENSG00000137409	chromatin interactions

Extended variants
information (count: 206 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:206 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527813980	chr6:36986712-36986713	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs547551541	chr6:36986740-36986741	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs567867130	chr6:36986762-36986763	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs536495448	chr6:36986806-36986807	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs556823712	chr6:36986855-36986856	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs149724900	chr6:36986866-36986867	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs1224487	chr6:36986917-36986918	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs184918870	chr6:36986925-36986926	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs146745510	chr6:36986975-36986976	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs34624708	chr6:36987048-36987049	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs370302844	chr6:36987112-36987113	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs139418516	chr6:36987131-36987132	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs73730515	chr6:36987146-36987147	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs573782671	chr6:36987162-36987163	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs189428492	chr6:36987175-36987176	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs28497343	chr6:36987217-36987218	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs146421614	chr6:36987225-36987226	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs531526983	chr6:36987245-36987246	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs544985964	chr6:36987273-36987274	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs539251083	chr6:36987333-36987334	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs192192429	chr6:36987363-36987364	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs546363545	chr6:36987388-36987389	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs9470455	chr6:36987483-36987484	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs149043087	chr6:36987492-36987493	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs184265218	chr6:36987579-36987580	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs143069858	chr6:36987596-36987597	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs200594484	chr6:36987627-36987628	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs200884693	chr6:36987631-36987632	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs397761943	chr6:36987646-36987647	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs831505	chr6:36987650-36987651	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs373030095	chr6:36987756-36987757	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs540506077	chr6:36987762-36987763	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs377598547	chr6:36987767-36987768	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs570344423	chr6:36987777-36987778	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs539377368	chr6:36987816-36987817	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189461519	chr6:36987833-36987834	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs375788141	chr6:36987846-36987847	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs112642340	chr6:36987889-36987890	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs140537622	chr6:36987908-36987909	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533825422	chr6:36987928-36987929	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560208927	chr6:36987964-36987965	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147092953	chr6:36987979-36987980	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs76336097	chr6:36987980-36987981	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs536423359	chr6:36987983-36987984	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs556119040	chr6:36988030-36988031	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575897056	chr6:36988040-36988041	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs544924606	chr6:36988041-36988042	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555506882	chr6:36988051-36988052	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs138516504	chr6:36988065-36988066	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs541105498	chr6:36988093-36988094	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	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
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36974200-36987000	Weak transcription	Right Atrium	heart
2	chr6:36975400-36988600	Weak transcription	Gastric	stomach
3	chr6:36975600-36988200	Weak transcription	Esophagus	oesophagus
4	chr6:36975600-36989600	Weak transcription	Thymus	Thymus
5	chr6:36983400-36995000	Weak transcription	Lung	lung
6	chr6:36984600-36987200	Enhancers	Fetal Thymus	thymus
7	chr6:36984800-36986800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr6:36984800-36987000	Enhancers	Brain Hippocampus Middle	brain
9	chr6:36984800-36987200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:36984800-36987200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:36984800-36989000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr6:36985000-36986800	Enhancers	Brain Substantia Nigra	brain
13	chr6:36985200-36987000	Enhancers	Fetal Muscle Leg	muscle
14	chr6:36985200-36987000	Enhancers	Placenta	Placenta
15	chr6:36985200-36987200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr6:36985200-36987400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:36985200-36987400	Enhancers	Brain Cingulate Gyrus	brain
18	chr6:36985200-36988200	Genic enhancers	Primary B cells from peripheral blood	blood
19	chr6:36985400-36987000	Genic enhancers	Primary monocytes fromperipheralblood	blood
20	chr6:36985400-36987000	Genic enhancers	Monocytes-CD14+_RO01746	blood
21	chr6:36985400-36987200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr6:36985400-36987200	Enhancers	Brain Angular Gyrus	brain
23	chr6:36985400-36987400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr6:36985400-36987400	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr6:36985400-36987400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr6:36985400-36987400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:36985400-36987400	Enhancers	Fetal Muscle Trunk	muscle
28	chr6:36985400-36987600	Enhancers	Brain Germinal Matrix	brain
29	chr6:36985600-36987000	Enhancers	Fetal Intestine Large	intestine
30	chr6:36985600-36987000	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr6:36985600-36987000	Genic enhancers	GM12878-XiMat	blood
32	chr6:36985600-36987200	Genic enhancers	Primary B cells from cord blood	blood
33	chr6:36985600-36987200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr6:36985600-36987200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr6:36985600-36987200	Enhancers	Brain Anterior Caudate	brain
36	chr6:36985600-36987200	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr6:36985600-36987200	Enhancers	HepG2	liver
38	chr6:36985600-36987200	Enhancers	K562	blood
39	chr6:36985600-36987400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:36985600-36987400	Enhancers	Primary T cells fromperipheralblood	blood
41	chr6:36985600-36987400	Enhancers	Primary hematopoietic stem cells	blood
42	chr6:36985600-36987400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:36985600-36987400	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr6:36985600-36987400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr6:36985600-36987400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr6:36985600-36987400	Enhancers	Colon Smooth Muscle	Colon
47	chr6:36985600-36987400	Enhancers	Fetal Stomach	stomach
48	chr6:36985600-36987600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr6:36985600-36987600	Enhancers	HMEC	breast
50	chr6:36985600-36988800	Enhancers	Fetal Heart	heart

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