Variant report

Variant	esv1807065
Chromosome Location	chr6:37379409-37399185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:232)
CpG islands
(count:122)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:232 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:37391417-37391979	K562	blood:	n/a	n/a
2	ATF1	chr6:37391504-37391835	K562	blood:	n/a	n/a
3	BACH1	chr6:37396733-37396933	K562	blood:	n/a	n/a
4	BCLAF1	chr6:37391465-37392158	K562	blood:	n/a	n/a
5	BCLAF1	chr6:37391454-37392096	K562	blood:	n/a	n/a
6	BHLHE40	chr6:37393067-37393383	K562	blood:	n/a	n/a
7	BHLHE40	chr6:37391547-37391699	K562	blood:	n/a	n/a
8	CBX3	chr6:37385182-37385505	K562	blood:	n/a	n/a
9	CBX3	chr6:37391274-37391997	K562	blood:	n/a	n/a
10	CBX3	chr6:37394167-37395205	K562	blood:	n/a	n/a
11	CBX3	chr6:37391383-37391956	K562	blood:	n/a	n/a
12	CBX3	chr6:37385115-37385531	K562	blood:	n/a	n/a
13	CCNT2	chr6:37391716-37391916	K562	blood:	n/a	n/a
14	CCNT2	chr6:37394498-37394951	K562	blood:	n/a	n/a
15	CEBPB	chr6:37392417-37392900	K562	blood:	n/a	n/a
16	CEBPB	chr6:37395698-37395777	K562	blood:	n/a	n/a
17	CEBPB	chr6:37391540-37391785	K562	blood:	n/a	n/a
18	CEBPB	chr6:37391487-37391941	K562	blood:	n/a	n/a
19	CEBPD	chr6:37391354-37392061	K562	blood:	n/a	n/a
20	CEBPD	chr6:37391451-37392106	K562	blood:	n/a	n/a
21	CHD2	chr6:37391207-37391836	K562	blood:	n/a	n/a
22	CTCF	chr6:37383584-37383627	GM10248	blood:	n/a	n/a
23	CTCF	chr6:37383629-37383634	GM10248	blood:	n/a	n/a
24	CTCF	chr6:37394380-37394530	HEK293	kidney:	n/a	n/a
25	CTCF	chr6:37391368-37391522	K562	blood:	n/a	n/a
26	CTCF	chr6:37383467-37383554	GM10266	blood:	n/a	n/a
27	CUX1	chr6:37391342-37391590	K562	blood:	n/a	n/a
28	E2F6	chr6:37394326-37394524	K562	blood:	n/a	n/a
29	E2F6	chr6:37394691-37395125	K562	blood:	n/a	n/a
30	E2F6	chr6:37393072-37393291	K562	blood:	n/a	n/a
31	EGR1	chr6:37392148-37392396	K562	blood:	n/a	n/a
32	EGR1	chr6:37392159-37392437	K562	blood:	n/a	n/a
33	ELF1	chr6:37391386-37391858	K562	blood:	n/a	n/a
34	EP300	chr6:37395729-37395786	K562	blood:	n/a	n/a
35	EP300	chr6:37396994-37397401	GM12878	blood:	n/a	n/a
36	EP300	chr6:37397262-37397491	K562	blood:	n/a	n/a
37	EP300	chr6:37391562-37391943	K562	blood:	n/a	n/a
38	EP300	chr6:37393888-37394009	GM12878	blood:	n/a	n/a
39	EP300	chr6:37395857-37396066	GM12878	blood:	n/a	n/a
40	EP300	chr6:37392422-37392634	GM12878	blood:	n/a	n/a
41	EP300	chr6:37393314-37393570	GM12878	blood:	n/a	n/a
42	EP300	chr6:37394765-37395331	GM12878	blood:	n/a	n/a
43	EP300	chr6:37379461-37379533	GM12878	blood:	n/a	n/a
44	EP300	chr6:37391254-37391926	GM12878	blood:	n/a	n/a
45	ETS1	chr6:37391548-37391938	K562	blood:	n/a	n/a
46	FAM48A	chr6:37394069-37394149	GM12878	blood:	n/a	n/a
47	FOXA1	chr6:37391449-37391874	T-47D	breast:	n/a	n/a
48	FOXA1	chr6:37391471-37391847	T-47D	breast:	n/a	n/a
49	GATA2	chr6:37388819-37389160	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr6:37395440-37395640	SH-SY5Y	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:37391769-37391819	H1-hESC	embryonic stem cell:	embryo
2	chr6:37391769-37391819	Hela-S3	cervix:	n/a
3	chr6:37391769-37391819	AG04450	lung:	fetal
4	chr6:37397886-37397936	GM12891	blood:	n/a
5	chr6:37397886-37397936	H1-hESC	embryonic stem cell:	embryo
6	chr6:37397886-37397936	U87	brain:	n/a
7	chr6:37397886-37397936	GM12878	blood:	n/a
8	chr6:37391769-37391819	MCF-7	breast:	n/a
9	chr6:37391769-37391819	BJ	skin:	n/a
10	chr6:37391769-37391819	PFSK-1	brain:	n/a
11	chr6:37397886-37397936	HCPEpiC	choroid plexus:	n/a
12	chr6:37397886-37397936	GM06990	blood:	n/a
13	chr6:37391769-37391819	U87	brain:	n/a
14	chr6:37391769-37391819	NHDF-neo	bronchial:	n/a
15	chr6:37397886-37397936	MCF-7	breast:	n/a
16	chr6:37391769-37391819	HRE	kidney:	n/a
17	chr6:37397886-37397936	BJ	skin:	n/a
18	chr6:37397886-37397936	A549	lung:	n/a
19	chr6:37391769-37391819	Jurkat	blood:	n/a
20	chr6:37391769-37391819	PrEC	prostate:	n/a
21	chr6:37391769-37391819	HepG2	liver:	n/a
22	chr6:37397886-37397936	PANC-1	pancreas:	n/a
23	chr6:37391769-37391819	HCT-116	colon:	n/a
24	chr6:37391769-37391819	HNPCEpiC	eye:	n/a
25	chr6:37391769-37391819	AG09309	skin:	n/a
26	chr6:37397886-37397936	HNPCEpiC	eye:	n/a
27	chr6:37397886-37397936	HRE	kidney:	n/a
28	chr6:37397886-37397936	HMEC	breast:	n/a
29	chr6:37397886-37397936	HCM	heart:	n/a
30	chr6:37391769-37391819	RPTEC	kidney:	n/a
31	chr6:37397886-37397936	AG04450	lung:	fetal
32	chr6:37397886-37397936	NB4	blood:	n/a
33	chr6:37397886-37397936	HRCEpiC	kidney:	n/a
34	chr6:37391769-37391819	NH-A	brain:	n/a
35	chr6:37391769-37391819	SK-N-SH	brain:	n/a
36	chr6:37391769-37391819	NB4	blood:	n/a
37	chr6:37397886-37397936	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:37391769-37391819	A549	lung:	n/a
39	chr6:37391769-37391819	HCM	heart:	n/a
40	chr6:37391769-37391819	MCF10A-Er-Src	breast:	n/a
41	chr6:37397886-37397936	AoSMC	blood vessel:	n/a
42	chr6:37397886-37397936	SK-N-SH	brain:	n/a
43	chr6:37397886-37397936	K562	blood:	n/a
44	chr6:37391769-37391819	NT2-D1	testis:	n/a
45	chr6:37391769-37391819	HEK293	kidney:	embryo
46	chr6:37391769-37391819	AG09319	gingival:	n/a
47	chr6:37397886-37397936	HL-60	blood:	n/a
48	chr6:37397886-37397936	PrEC	prostate:	n/a
49	chr6:37391769-37391819	ovcar-3	ovarian:	n/a
50	chr6:37391769-37391819	HRPEpiC	eye:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:37368034..37370544-chr6:37386346..37388748,2	K562	blood:
2	chr6:37383701..37387029-chr6:37388839..37391915,5	K562	blood:
3	chr6:37348302..37351113-chr6:37394191..37396575,2	K562	blood:
4	chr6:37389971..37393834-chr6:37440150..37443110,4	MCF-7	breast:
5	chr6:37384249..37387029-chr6:37388839..37391579,3	K562	blood:
6	chr6:37391896..37393452-chr6:37438457..37441158,2	K562	blood:
7	chr6:37326963..37329509-chr6:37395031..37398456,3	K562	blood:
8	chr6:37349539..37351113-chr6:37394191..37396752,2	K562	blood:
9	chr6:37383701..37387029-chr6:37388839..37391915,5	K562	blood:
10	chr6:37384249..37387029-chr6:37388839..37391579,3	K562	blood:
11	chr12:57472395..57472910-chr6:37391804..37392346,2	MCF-7	breast:
12	chr6:37364657..37367034-chr6:37394152..37396378,2	K562	blood:
13	chr6:37366536..37368392-chr6:37392528..37396420,3	K562	blood:
14	chr6:37382160..37383794-chr6:37394542..37397264,2	K562	blood:
15	chr6:37392263..37395409-chr6:37412629..37415266,3	K562	blood:
16	chr6:37394541..37397125-chr6:37465696..37468350,2	K562	blood:
17	chr6:37391746..37394017-chr6:37438131..37441075,2	MCF-7	breast:
18	chr6:37395898..37398145-chr6:37408899..37411047,2	K562	blood:
19	chr20:52278366..52278868-chr6:37379498..37380000,2	MCF-7	breast:
20	chr6:37387252..37388819-chr6:37391241..37393243,2	K562	blood:
21	chr6:37394420..37396941-chr6:37406816..37408939,3	K562	blood:
22	chr6:37341724..37343636-chr6:37392718..37394515,2	K562	blood:
23	chr6:37322263..37324339-chr6:37389226..37391465,2	MCF-7	breast:
24	chr6:37393592..37395847-chr6:37407900..37409924,2	K562	blood:
25	chr6:37376102..37378184-chr6:37397531..37399649,2	K562	blood:
26	chr6:37396986..37398925-chr6:37399222..37402219,2	MCF-7	breast:
27	chr6:37378517..37380520-chr6:37381808..37383680,2	K562	blood:
28	chr6:37379072..37381849-chr6:37391515..37393153,2	MCF-7	breast:
29	chr6:37386436..37388168-chr6:37390589..37393996,3	MCF-7	breast:
30	chr6:37393552..37395813-chr6:37520408..37522475,2	K562	blood:
31	chr6:37290599..37292900-chr6:37390289..37392598,3	K562	blood:
32	chr6:37379072..37381849-chr6:37391515..37393153,2	MCF-7	breast:
33	chr6:37390262..37393860-chr6:37393896..37398106,6	MCF-7	breast:
34	chr6:37393939..37397239-chr6:37426507..37429534,4	K562	blood:
35	chr6:37393178..37396451-chr6:37404709..37407721,4	K562	blood:
36	chr6:37391025..37394535-chr6:37463764..37466076,3	K562	blood:
37	chr6:37336070..37337842-chr6:37390532..37393304,2	K562	blood:
38	chr6:37378517..37380520-chr6:37381808..37383680,2	K562	blood:
39	chr6:37375004..37377586-chr6:37391098..37392841,2	MCF-7	breast:
40	chr6:37391025..37393237-chr6:37463835..37465802,2	K562	blood:
41	chr6:37387252..37388819-chr6:37391241..37393243,2	K562	blood:
42	chr6:37391738..37394075-chr6:37408772..37412559,3	K562	blood:
43	chr6:37386436..37388168-chr6:37390589..37393996,3	MCF-7	breast:
44	chr6:37390262..37393860-chr6:37393896..37398106,6	MCF-7	breast:
45	chr6:37326963..37328808-chr6:37396406..37398456,2	K562	blood:
46	chr6:37388900..37391581-chr6:37403584..37406042,2	MCF-7	breast:
47	chr6:37370276..37372478-chr6:37392571..37394863,2	K562	blood:
48	chr6:37385441..37389491-chr6:37393675..37396970,4	K562	blood:
49	chr6:37385441..37389491-chr6:37393675..37396970,4	K562	blood:
50	chr6:37391304..37393328-chr6:37535749..37538149,2	MCF-7	breast:

No data

Variant related genes	Relation type
CMTR1	TF binding region
CMTR1	CpG island
ENSG00000166881	chromatin interactions
ENSG00000239953	chromatin interactions
ENSG00000198937	chromatin interactions
ENSG00000112130	chromatin interactions
ENSG00000137200	chromatin interactions

Extended variants
information (count: 356 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567113960	chr6:37386807-37386808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs377315328	chr6:37386836-37386837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192787899	chr6:37386839-37386840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143471864	chr6:37386868-37386869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576313166	chr6:37386902-37386903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568892065	chr6:37386911-37386912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146770575	chr6:37386951-37386952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140070050	chr6:37386978-37386979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572404882	chr6:37386988-37386989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527831846	chr6:37387159-37387160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201197870	chr6:37389971-37389972	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs9380667	chr6:37389972-37389973	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs9394435	chr6:37389981-37389982	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs9380668	chr6:37389989-37389990	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530516798	chr6:37389996-37389997	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550387029	chr6:37389999-37390000	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200818511	chr6:37390000-37390001	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201283252	chr6:37390001-37390002	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201352639	chr6:37390002-37390003	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs9380670	chr6:37390003-37390004	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373255263	chr6:37390005-37390006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566761390	chr6:37390026-37390027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186696549	chr6:37390189-37390190	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143407201	chr6:37390193-37390194	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2776917	chr6:37390211-37390212	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs367876215	chr6:37390217-37390218	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547937432	chr6:37390221-37390222	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148485747	chr6:37390225-37390226	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190681952	chr6:37390245-37390246	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs34380526	chr6:37390262-37390263	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs578194862	chr6:37390294-37390295	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201577851	chr6:37390301-37390302	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534227232	chr6:37390303-37390304	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530126117	chr6:37390305-37390306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs76253741	chr6:37390306-37390307	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371388456	chr6:37390313-37390314	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532546514	chr6:37390320-37390321	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs547739076	chr6:37390362-37390363	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4714066	chr6:37390372-37390373	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs554920138	chr6:37390406-37390407	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs536424370	chr6:37390410-37390411	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs150932160	chr6:37390432-37390433	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538995039	chr6:37390521-37390522	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs543868130	chr6:37390531-37390532	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs79783237	chr6:37390548-37390549	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs140756366	chr6:37390567-37390568	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs533110055	chr6:37390568-37390569	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540044407	chr6:37390618-37390619	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs182878032	chr6:37390631-37390632	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs529157109	chr6:37390656-37390657	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37386800-37387200	Enhancers	Fetal Intestine Large	intestine
2	chr6:37386800-37387200	Enhancers	Fetal Intestine Small	intestine
3	chr6:37390800-37391000	Enhancers	K562	blood
4	chr6:37391000-37391600	Flanking Active TSS	K562	blood
5	chr6:37391600-37393200	Active TSS	K562	blood
6	chr6:37391800-37392400	Active TSS	Placenta	Placenta
7	chr6:37393200-37394600	Flanking Active TSS	K562	blood
8	chr6:37394600-37394800	Active TSS	Duodenum Mucosa	Duodenum
9	chr6:37394600-37395000	Transcr. at gene 5' and 3'	K562	blood
10	chr6:37394600-37395200	Enhancers	HepG2	liver
11	chr6:37394800-37395000	Flanking Active TSS	Duodenum Mucosa	Duodenum
12	chr6:37395000-37395200	Enhancers	Duodenum Mucosa	Duodenum
13	chr6:37395000-37396200	Flanking Active TSS	K562	blood
14	chr6:37395200-37400000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr6:37395200-37400000	Weak transcription	HepG2	liver
16	chr6:37395800-37396200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:37396000-37396200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:37396000-37396200	Enhancers	NHEK	skin
19	chr6:37396200-37398000	Enhancers	K562	blood
20	chr6:37396200-37400200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:37398000-37399000	Weak transcription	K562	blood
22	chr6:37398000-37400200	Weak transcription	HSMMtube	muscle
23	chr6:37399000-37400200	Enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links