Variant report

Variant	nsv969392
Chromosome Location	chr6:37052594-37060796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:37059596-37059640	K562	blood:	n/a	n/a
2	BHLHE40	chr6:37059554-37059746	HepG2	liver:	n/a	n/a
3	BRCA1	chr6:37059454-37059772	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:37054188-37054460	HepG2	liver:	n/a	chr6:37054322-37054333
5	CEBPB	chr6:37054157-37054502	K562	blood:	n/a	chr6:37054322-37054333
6	CEBPB	chr6:37053678-37053847	Hela-S3	cervix:	n/a	chr6:37053745-37053758
7	CEBPB	chr6:37054190-37054489	IMR90	lung:	n/a	chr6:37054322-37054333
8	CEBPB	chr6:37054200-37054498	Hela-S3	cervix:	n/a	chr6:37054322-37054333
9	CEBPB	chr6:37054260-37054454	A549	lung:	n/a	chr6:37054322-37054333
10	CEBPB	chr6:37053686-37053846	K562	blood:	n/a	chr6:37053745-37053758
11	CEBPB	chr6:37059497-37059699	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:37059438-37059855	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr6:37057442-37057534	K562	blood:	n/a	n/a
14	CTCF	chr6:37056820-37056970	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr6:37057540-37057690	GM12875	blood:	n/a	n/a
16	CTCF	chr6:37056860-37057010	NHDF-neo	bronchial:	n/a	n/a
17	EP300	chr6:37059452-37059655	Hela-S3	cervix:	n/a	chr6:37059624-37059638
18	ESR1	chr6:37060766-37061082	ECC-1	luminal epithelium:	n/a	n/a
19	FOS	chr6:37053634-37053853	MCF10A-Er-Src	breast:	n/a	chr6:37053723-37053733 chr6:37053724-37053732
20	FOS	chr6:37053670-37053837	MCF10A-Er-Src	breast:	n/a	chr6:37053723-37053733 chr6:37053724-37053732
21	GATA3	chr6:37056668-37056868	SH-SY5Y	brain:	n/a	n/a
22	HNF4A	chr6:37058899-37059191	HepG2	liver:	n/a	chr6:37059022-37059035 chr6:37059019-37059037 chr6:37059020-37059035 chr6:37059022-37059034 chr6:37059022-37059034 chr6:37059021-37059036
23	HNF4A	chr6:37058916-37059258	HepG2	liver:	n/a	chr6:37059022-37059035 chr6:37059019-37059037 chr6:37059020-37059035 chr6:37059022-37059034 chr6:37059022-37059034 chr6:37059021-37059036
24	HNF4G	chr6:37058945-37059179	HepG2	liver:	n/a	chr6:37059022-37059035 chr6:37059019-37059034 chr6:37059019-37059037 chr6:37059022-37059034 chr6:37059022-37059034 chr6:37059021-37059036
25	IRF1	chr6:37056688-37056736	K562	blood:	n/a	n/a
26	KAP1	chr6:37059551-37059809	U2OS	brain:	n/a	n/a
27	MAX	chr6:37059322-37059827	Hela-S3	cervix:	n/a	n/a
28	MAX	chr6:37060621-37061288	K562	blood:	n/a	n/a
29	MAX	chr6:37059429-37059858	Hela-S3	cervix:	n/a	n/a
30	MXI1	chr6:37059525-37059843	Hela-S3	cervix:	n/a	n/a
31	MYC	chr6:37059455-37059847	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr6:37056681-37056846	K562	blood:	n/a	n/a
33	POLR2A	chr6:37052341-37052789	K562	blood:	n/a	n/a
34	POLR2A	chr6:37059130-37059329	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr6:37060493-37060778	K562	blood:	n/a	n/a
36	POLR2A	chr6:37060380-37060508	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr6:37052989-37053603	K562	blood:	n/a	n/a
38	POLR2A	chr6:37056168-37056201	K562	blood:	n/a	n/a
39	POU2F2	chr6:37059347-37059659	GM12878	blood:	n/a	n/a
40	RCOR1	chr6:37053817-37054077	K562	blood:	n/a	n/a
41	RCOR1	chr6:37053874-37053921	K562	blood:	n/a	n/a
42	RFX5	chr6:37059426-37059843	Hela-S3	cervix:	n/a	n/a
43	SMC3	chr6:37059451-37059688	Hela-S3	cervix:	n/a	n/a
44	STAT3	chr6:37059632-37059651	MCF10A-Er-Src	breast:	n/a	n/a
45	TCF12	chr6:37056567-37057053	SK-N-SH	brain:	n/a	n/a
46	TCF7L2	chr6:37059426-37059772	Hela-S3	cervix:	n/a	n/a
47	USF2	chr6:37059542-37059826	Hela-S3	cervix:	n/a	chr6:37059704-37059715
48	YY1	chr6:37059412-37059540	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:37060693-37060743	H1-hESC	embryonic stem cell:	embryo
2	chr6:37060693-37060743	NH-A	brain:	n/a
3	chr6:37060693-37060743	BE2_C	brain:	n/a
4	chr6:37060693-37060743	HCPEpiC	choroid plexus:	n/a
5	chr6:37060693-37060743	K562	blood:	n/a
6	chr6:37060693-37060743	AG09319	gingival:	n/a
7	chr6:37060693-37060743	HRE	kidney:	n/a
8	chr6:37060693-37060743	AoSMC	blood vessel:	n/a
9	chr6:37060693-37060743	HRCEpiC	kidney:	n/a
10	chr6:37060693-37060743	PFSK-1	brain:	n/a
11	chr6:37060693-37060743	NT2-D1	testis:	n/a
12	chr6:37060693-37060743	MCF-7	breast:	n/a
13	chr6:37060693-37060743	SK-N-SH	brain:	n/a
14	chr6:37060693-37060743	ovcar-3	ovarian:	n/a
15	chr6:37060693-37060743	HMEC	breast:	n/a
16	chr6:37060693-37060743	GM06990	blood:	n/a
17	chr6:37060693-37060743	SKMC	muscle:	n/a
18	chr6:37060693-37060743	HEK293	kidney:	embryo
19	chr6:37060693-37060743	HIPEpiC	eye:	n/a
20	chr6:37060693-37060743	U87	brain:	n/a
21	chr6:37060693-37060743	AG10803	skin:	n/a
22	chr6:37060693-37060743	HCF	heart:	n/a
23	chr6:37060693-37060743	GM12891	blood:	n/a
24	chr6:37060693-37060743	HL-60	blood:	n/a
25	chr6:37060693-37060743	HAEpiC	amniotic membrane:	n/a
26	chr6:37060693-37060743	Jurkat	blood:	n/a
27	chr6:37060693-37060743	NB4	blood:	n/a
28	chr6:37060693-37060743	RPTEC	kidney:	n/a
29	chr6:37060693-37060743	GM12892	blood:	n/a
30	chr6:37060693-37060743	A549	lung:	n/a
31	chr6:37060693-37060743	ECC-1	luminal epithelium:	n/a
32	chr6:37060693-37060743	GM19239	blood:	n/a
33	chr6:37060693-37060743	PrEC	prostate:	n/a
34	chr6:37060693-37060743	BJ	skin:	n/a
35	chr6:37060693-37060743	HUVEC	blood vessel:	n/a
36	chr6:37060693-37060743	AG09309	skin:	n/a
37	chr6:37060693-37060743	NHBE	bronchial:	n/a
38	chr6:37060693-37060743	MCF10A-Er-Src	breast:	n/a
39	chr6:37060693-37060743	Hela-S3	cervix:	n/a
40	chr6:37060693-37060743	Caco-2	colon:	n/a
41	chr6:37060693-37060743	HRPEpiC	eye:	n/a
42	chr6:37060693-37060743	HCM	heart:	n/a
43	chr6:37060693-37060743	AG04450	lung:	fetal
44	chr6:37060693-37060743	AG04449	skin:	fetal
45	chr6:37060693-37060743	SAEC	small airway:	n/a
46	chr6:37060693-37060743	LNCaP	prostate:	n/a
47	chr6:37060693-37060743	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:37060693-37060743	CMK	blood:	n/a
49	chr6:37060693-37060743	ProgFib	skin:	n/a
50	chr6:37060693-37060743	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:37027099..37030994-chr6:37049896..37053173,4	MCF-7	breast:
2	chr6:37060206..37065655-chr6:37067548..37072519,8	K562	blood:
3	chr6:37055918..37058641-chr6:37136878..37140744,5	K562	blood:
4	chr6:37027478..37029052-chr6:37051959..37053874,2	MCF-7	breast:
5	chr6:37054904..37056692-chr6:37060805..37062667,2	K562	blood:
6	chr6:37043566..37047908-chr6:37051801..37055072,4	MCF-7	breast:
7	chr6:37056453..37058163-chr6:37061494..37063328,2	K562	blood:
8	chr6:37040241..37044221-chr6:37049851..37052927,3	K562	blood:
9	chr6:37050093..37053026-chr6:37139819..37142668,2	K562	blood:

Variant related genes	Relation type
RPL12P2	TF binding region
RPL12P2	CpG island
ENSG00000137193	chromatin interactions

Extended variants
information (count: 381 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:381 , 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	rs373181942	chr6:37052611-37052612	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs7751821	chr6:37052612-37052613	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs11970215	chr6:37052667-37052668	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372337712	chr6:37052672-37052673	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375433301	chr6:37052720-37052721	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532780382	chr6:37052736-37052737	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546259527	chr6:37052764-37052765	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs114451176	chr6:37052765-37052766	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371673763	chr6:37052770-37052771	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529016021	chr6:37052775-37052776	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148115653	chr6:37052776-37052777	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190577711	chr6:37052793-37052794	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531597593	chr6:37052808-37052809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371046430	chr6:37052829-37052830	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551718391	chr6:37052845-37052846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571641576	chr6:37052852-37052853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534163806	chr6:37052853-37052854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs141233737	chr6:37052889-37052890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs182413217	chr6:37052899-37052900	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536799928	chr6:37052906-37052907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs11964406	chr6:37052919-37052920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs556434978	chr6:37052941-37052942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs576587423	chr6:37052946-37052947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545262782	chr6:37052997-37052998	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558844164	chr6:37053007-37053008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187022256	chr6:37053034-37053035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375036928	chr6:37053061-37053062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369230356	chr6:37053096-37053097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112476934	chr6:37053129-37053130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191101206	chr6:37053133-37053134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571980341	chr6:37053192-37053193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528975174	chr6:37053209-37053210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374463396	chr6:37053227-37053228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372016452	chr6:37053243-37053244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542707603	chr6:37053293-37053294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375141273	chr6:37053317-37053318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139168861	chr6:37053334-37053335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531560480	chr6:37053342-37053343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369666007	chr6:37053348-37053349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs58954992	chr6:37053349-37053350	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs146039666	chr6:37053350-37053351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537884567	chr6:37053358-37053359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139799189	chr6:37053360-37053361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377424153	chr6:37053388-37053389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367772243	chr6:37053404-37053405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182117231	chr6:37053416-37053417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369025004	chr6:37053423-37053424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554527248	chr6:37053447-37053448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143185029	chr6:37053484-37053485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373217470	chr6:37053490-37053491	Weak transcription Enhancers	n/a	n/a	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37045800-37060800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:37048800-37052600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr6:37049600-37052800	Enhancers	Fetal Intestine Large	intestine
4	chr6:37049600-37053200	Enhancers	Fetal Intestine Small	intestine
5	chr6:37050400-37052600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr6:37050400-37053200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr6:37050600-37052600	Enhancers	Primary hematopoietic stem cells	blood
8	chr6:37050600-37052800	Enhancers	Ovary	ovary
9	chr6:37050800-37052800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr6:37050800-37054000	Enhancers	Spleen	Spleen
11	chr6:37051200-37052600	Enhancers	Primary B cells from cord blood	blood
12	chr6:37051200-37052800	Enhancers	Liver	Liver
13	chr6:37051400-37052600	Weak transcription	Fetal Muscle Leg	muscle
14	chr6:37051400-37054600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr6:37051400-37060400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr6:37051600-37052600	Weak transcription	Esophagus	oesophagus
17	chr6:37051600-37053200	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr6:37051600-37053800	Weak transcription	Lung	lung
19	chr6:37051600-37054000	Enhancers	HepG2	liver
20	chr6:37051600-37060600	Weak transcription	A549	lung
21	chr6:37051600-37063400	Weak transcription	Small Intestine	intestine
22	chr6:37051800-37054000	Enhancers	K562	blood
23	chr6:37051800-37054400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:37051800-37056400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:37051800-37056600	Weak transcription	Fetal Stomach	stomach
26	chr6:37051800-37056600	Weak transcription	NHDF-Ad	bronchial
27	chr6:37051800-37056800	Weak transcription	Stomach Mucosa	stomach
28	chr6:37051800-37059000	Weak transcription	Hela-S3	cervix
29	chr6:37051800-37060600	Weak transcription	Pancreas	Pancrea
30	chr6:37052200-37053600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr6:37052200-37060600	Weak transcription	Adipose Nuclei	Adipose
32	chr6:37052200-37070000	Weak transcription	Right Atrium	heart
33	chr6:37052400-37053400	Weak transcription	Placenta	Placenta
34	chr6:37052400-37056600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:37052600-37052800	Enhancers	Esophagus	oesophagus
36	chr6:37052600-37052800	Enhancers	Fetal Muscle Leg	muscle
37	chr6:37052600-37054600	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr6:37052600-37056200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr6:37052800-37054400	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr6:37052800-37056400	Weak transcription	Fetal Intestine Large	intestine
41	chr6:37052800-37069800	Weak transcription	Ovary	ovary
42	chr6:37053200-37060400	Weak transcription	Fetal Intestine Small	intestine
43	chr6:37053400-37054200	Enhancers	Placenta	Placenta
44	chr6:37053600-37053800	Enhancers	Duodenum Mucosa	Duodenum
45	chr6:37053800-37054000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr6:37053800-37054000	Enhancers	Lung	lung
47	chr6:37054000-37054200	Weak transcription	Spleen	Spleen
48	chr6:37054000-37055600	Weak transcription	HepG2	liver
49	chr6:37054000-37056400	Weak transcription	K562	blood
50	chr6:37054200-37059000	Weak transcription	Placenta	Placenta

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