Variant report

Variant	nsv970069
Chromosome Location	chr6:144819-155708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:455)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:455 , 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	ATF1	chr6:148754-148953	K562	blood:	n/a	n/a
2	ATF1	chr6:148499-148519	K562	blood:	n/a	n/a
3	ATF2	chr6:154306-155179	GM12878	blood:	n/a	n/a
4	ATF2	chr6:148471-148923	GM12878	blood:	n/a	n/a
5	ATF2	chr6:154275-155106	GM12878	blood:	n/a	n/a
6	ATF2	chr6:152980-153487	GM12878	blood:	n/a	n/a
7	ATF2	chr6:150091-150623	GM12878	blood:	n/a	n/a
8	ATF3	chr6:148446-148924	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr6:148591-148922	GM12878	blood:	n/a	n/a
10	ATF3	chr6:148231-148982	GM12878	blood:	n/a	n/a
11	ATF3	chr6:148311-148978	K562	blood:	n/a	n/a
12	ATF3	chr6:148327-148589	GM12878	blood:	n/a	n/a
13	ATF3	chr6:148318-148914	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr6:148638-148982	GM12878	blood:	n/a	n/a
15	BATF	chr6:154197-154629	GM12878	blood:	n/a	n/a
16	BATF	chr6:147764-147960	GM12878	blood:	n/a	n/a
17	BATF	chr6:148266-149086	GM12878	blood:	n/a	n/a
18	BATF	chr6:154252-155133	GM12878	blood:	n/a	n/a
19	BATF	chr6:150238-150522	GM12878	blood:	n/a	n/a
20	BATF	chr6:152968-153416	GM12878	blood:	n/a	chr6:153318-153326
21	BATF	chr6:154691-155030	GM12878	blood:	n/a	n/a
22	BATF	chr6:153034-153312	GM12878	blood:	n/a	n/a
23	BATF	chr6:149172-149482	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:148334-148855	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:154309-155065	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:153082-153258	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:149231-149411	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:152949-153344	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:148308-149068	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:147742-147991	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:147772-148018	GM12878	blood:	n/a	n/a
32	BCL3	chr6:154271-155009	GM12878	blood:	n/a	n/a
33	BCL3	chr6:154627-155012	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:154574-155179	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:148262-149115	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:150190-150521	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:148500-149028	K562	blood:	n/a	n/a
38	BCLAF1	chr6:148303-148994	GM12878	blood:	n/a	n/a
39	BHLHE40	chr6:150404-150407	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:153089-153429	GM12878	blood:	n/a	n/a
41	BHLHE40	chr6:148386-148953	GM12878	blood:	n/a	n/a
42	BHLHE40	chr6:148483-148950	K562	blood:	n/a	n/a
43	CBX3	chr6:147719-149437	K562	blood:	n/a	n/a
44	CBX3	chr6:147664-149413	K562	blood:	n/a	n/a
45	CEBPB	chr6:148360-148854	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr6:148758-148949	GM12878	blood:	n/a	n/a
47	CEBPB	chr6:152500-152700	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:152577-152790	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:148330-149026	K562	blood:	n/a	n/a
50	CEBPB	chr6:148245-149261	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:148299-148349	AG10803	skin:	n/a
2	chr6:148112-148162	NT2-D1	testis:	n/a
3	chr6:148112-148162	SK-N-SH_RA	brain:	n/a
4	chr6:148299-148349	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:148299-148349	NH-A	brain:	n/a
6	chr6:148112-148162	NHBE	bronchial:	n/a
7	chr6:148112-148162	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:148299-148349	ECC-1	luminal epithelium:	n/a
9	chr6:148112-148162	GM12891	blood:	n/a
10	chr6:148299-148349	HNPCEpiC	eye:	n/a
11	chr6:148299-148349	AG04450	lung:	fetal
12	chr6:148299-148349	HEEpiC	esophagus:	n/a
13	chr6:148299-148349	ovcar-3	ovarian:	n/a
14	chr6:148299-148349	NB4	blood:	n/a
15	chr6:148299-148349	HEK293	kidney:	embryo
16	chr6:148112-148162	HCPEpiC	choroid plexus:	n/a
17	chr6:148112-148162	HRCEpiC	kidney:	n/a
18	chr6:148299-148349	Jurkat	blood:	n/a
19	chr6:148299-148349	CMK	blood:	n/a
20	chr6:148112-148162	SAEC	small airway:	n/a
21	chr6:148299-148349	H1-hESC	embryonic stem cell:	embryo
22	chr6:148112-148162	HUVEC	blood vessel:	n/a
23	chr6:148299-148349	GM12891	blood:	n/a
24	chr6:148112-148162	PFSK-1	brain:	n/a
25	chr6:148112-148162	MCF-7	breast:	n/a
26	chr6:148299-148349	ProgFib	skin:	n/a
27	chr6:148112-148162	HMEC	breast:	n/a
28	chr6:148299-148349	HRPEpiC	eye:	n/a
29	chr6:148112-148162	ProgFib	skin:	n/a
30	chr6:148299-148349	HRE	kidney:	n/a
31	chr6:148112-148162	HIPEpiC	eye:	n/a
32	chr6:148299-148349	PANC-1	pancreas:	n/a
33	chr6:148112-148162	HCT-116	colon:	n/a
34	chr6:148112-148162	HRE	kidney:	n/a
35	chr6:148112-148162	Jurkat	blood:	n/a
36	chr6:148112-148162	HCM	heart:	n/a
37	chr6:148112-148162	HRPEpiC	eye:	n/a
38	chr6:148112-148162	NH-A	brain:	n/a
39	chr6:148112-148162	SK-N-MC	brain:	n/a
40	chr6:148299-148349	BJ	skin:	n/a
41	chr6:148112-148162	HCF	heart:	n/a
42	chr6:148299-148349	PrEC	prostate:	n/a
43	chr6:148112-148162	HEEpiC	esophagus:	n/a
44	chr6:148112-148162	U87	brain:	n/a
45	chr6:148299-148349	AG09309	skin:	n/a
46	chr6:148112-148162	HNPCEpiC	eye:	n/a
47	chr6:148112-148162	BE2_C	brain:	n/a
48	chr6:148112-148162	Caco-2	colon:	n/a
49	chr6:148299-148349	HUVEC	blood vessel:	n/a
50	chr6:148112-148162	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:62916743..62917542-chr6:148260..148788,5	MCF-7	breast:
2	chr20:62916814..62917490-chr6:147992..148792,5	K562	blood:
3	chr20:62916965..62917673-chr6:148286..148790,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOC2-7	chr6:147400-147590	NR_109817
2	lnc-EXOC2-7	chr6:148025-148159	NR_109817
3	lnc-AL035696.1-5	chr6:155135-155395	XLOC_005116

No data

Variant related genes	Relation type
CICP18	TF binding region
LINC00266-3	TF binding region
CICP18	CpG island
LINC00266-3	CpG island

Extended variants
information (count: 233 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:233 , 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	rs199852223	chr6:145563-145564	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs550217298	chr6:145579-145580	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs77207585	chr6:145615-145616	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs371624296	chr6:146889-146890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs28402781	chr6:146890-146891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200869127	chr6:146923-146924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368166100	chr6:147032-147033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113579693	chr6:147099-147100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199560763	chr6:147236-147237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113387272	chr6:147238-147239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200399612	chr6:147332-147333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12530400	chr6:147404-147405	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs373481990	chr6:147489-147490	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs12524629	chr6:147564-147565	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs141507289	chr6:147596-147597	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs146227243	chr6:147646-147647	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs529613262	chr6:147651-147652	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs372297409	chr6:147666-147667	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs13217349	chr6:147671-147672	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs62388675	chr6:147687-147688	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs62388676	chr6:147688-147689	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs12525498	chr6:147691-147692	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs12526701	chr6:147704-147705	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs370918789	chr6:147708-147709	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs13199645	chr6:147712-147713	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs200892315	chr6:147726-147727	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs62388677	chr6:147729-147730	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs62388678	chr6:147744-147745	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs202009574	chr6:147748-147749	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs62388679	chr6:147750-147751	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs62388680	chr6:147754-147755	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs149827228	chr6:147768-147769	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs201744030	chr6:147775-147776	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs199585512	chr6:147778-147779	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs200765206	chr6:147781-147782	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs201992773	chr6:147793-147794	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs146245562	chr6:147815-147816	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs368782723	chr6:147816-147817	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs373924663	chr6:147841-147842	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs70982821	chr6:147843-147844	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs144760592	chr6:147844-147845	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs148590899	chr6:147845-147846	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs142956250	chr6:147847-147848	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs113872396	chr6:147848-147849	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs377753523	chr6:147868-147869	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs142361124	chr6:147869-147870	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs200160087	chr6:147891-147892	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs139613578	chr6:147908-147909	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs200050963	chr6:147909-147910	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs147914738	chr6:147912-147913	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Prader-willi syndrome	20588305	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495311	CNVD
small cell lung cancer	20016488	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	20435627	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146800-147800	Weak transcription	Right Atrium	heart
2	chr6:147600-148000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:147600-148200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
4	chr6:147800-148800	Strong transcription	Right Atrium	heart
5	chr6:148000-148400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:148800-150400	Weak transcription	Right Atrium	heart
7	chr6:149400-150800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
8	chr6:149400-151000	Enhancers	Thymus	Thymus
9	chr6:149400-154200	Enhancers	GM12878-XiMat	blood
10	chr6:149600-149800	Enhancers	Fetal Thymus	thymus
11	chr6:149800-153400	Weak transcription	Fetal Thymus	thymus
12	chr6:150200-150800	Enhancers	Primary T cells from cord blood	blood
13	chr6:150200-151000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:150400-150800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:151000-151400	Weak transcription	Thymus	Thymus
16	chr6:151400-152000	Enhancers	Thymus	Thymus
17	chr6:151800-152400	Enhancers	Placenta	Placenta
18	chr6:151800-155200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:151800-155600	Enhancers	HMEC	breast
20	chr6:152000-153200	Weak transcription	Thymus	Thymus
21	chr6:152400-154000	Weak transcription	Placenta	Placenta
22	chr6:152800-153600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:153000-153400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:153000-155000	Enhancers	NHEK	skin
25	chr6:153200-153800	Enhancers	Thymus	Thymus
26	chr6:153400-154000	Enhancers	Fetal Thymus	thymus
27	chr6:153400-154800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:153600-154600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:153800-154200	Weak transcription	Thymus	Thymus
30	chr6:153800-154200	Enhancers	NHDF-Ad	bronchial
31	chr6:153800-157400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr6:154000-155800	Weak transcription	Fetal Thymus	thymus
33	chr6:154000-157000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:154200-154400	Enhancers	Placenta	Placenta
35	chr6:154200-154400	Enhancers	Thymus	Thymus
36	chr6:154200-154400	Flanking Active TSS	GM12878-XiMat	blood
37	chr6:154200-154600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr6:154200-155000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:154200-156200	Weak transcription	NHDF-Ad	bronchial
40	chr6:154400-154600	Enhancers	GM12878-XiMat	blood
41	chr6:154400-156200	Weak transcription	Thymus	Thymus
42	chr6:154600-155000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:154600-155200	Flanking Active TSS	GM12878-XiMat	blood
44	chr6:154600-155200	Enhancers	Osteobl	bone
45	chr6:154600-156200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:155000-155200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr6:155000-155200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr6:155000-155200	Enhancers	NHLF	lung
49	chr6:155200-156200	Weak transcription	NHLF	lung
50	chr6:155200-156400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links