Variant report

Variant	esv2756870
Chromosome Location	chr1:170315081-170413292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:222)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:222 , 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	BACH1	chr1:170412497-170412606	K562	blood:	n/a	n/a
2	BATF	chr1:170323768-170324161	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:170323834-170324095	GM12878	blood:	n/a	n/a
4	CEBPB	chr1:170354950-170355192	Hela-S3	cervix:	n/a	chr1:170355032-170355043
5	CEBPB	chr1:170346974-170347263	HepG2	liver:	n/a	chr1:170347126-170347137
6	CEBPB	chr1:170344834-170345027	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:170379582-170379941	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:170346972-170347258	IMR90	lung:	n/a	chr1:170347126-170347137
9	CEBPB	chr1:170346977-170347172	K562	blood:	n/a	chr1:170347126-170347137
10	CEBPB	chr1:170354892-170355129	HepG2	liver:	n/a	chr1:170355032-170355043
11	CTCF	chr1:170406160-170406310	SAEC	small airway:	n/a	n/a
12	CTCF	chr1:170324560-170324710	AG04450	lung:	n/a	n/a
13	CTCF	chr1:170406120-170406270	GM12878	blood:	n/a	n/a
14	CTCF	chr1:170406120-170406270	HCFaa	heart:	n/a	n/a
15	CTCF	chr1:170406140-170406290	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr1:170350487-170350563	LNCaP	prostate:	n/a	n/a
17	CTCF	chr1:170406140-170406290	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr1:170324680-170324830	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr1:170406122-170406379	IMR90	lung:	n/a	n/a
20	CTCF	chr1:170406240-170406390	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr1:170406202-170406297	Lung_OC	lung:	n/a	n/a
22	CTCF	chr1:170406120-170406270	AG04449	skin:	n/a	n/a
23	CTCF	chr1:170338676-170338855	MCF-7	breast:	n/a	n/a
24	CTCF	chr1:170338706-170338827	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:170406180-170406330	HMEC	breast:	n/a	n/a
26	CTCF	chr1:170406180-170406330	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr1:170373640-170373790	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr1:170406120-170406270	AG04450	lung:	n/a	n/a
29	CTCF	chr1:170406174-170406271	Medullo	brain:	n/a	n/a
30	CTCF	chr1:170406140-170406358	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr1:170406140-170406290	HCM	heart:	n/a	n/a
32	CTCF	chr1:170316160-170316310	AG09309	skin:	n/a	n/a
33	CTCF	chr1:170324560-170324710	HMF	breast:	n/a	n/a
34	CTCF	chr1:170406160-170406310	HMF	breast:	n/a	n/a
35	CTCF	chr1:170324480-170324630	AG04450	lung:	n/a	n/a
36	CTCF	chr1:170406199-170406249	NHEK	skin:	n/a	n/a
37	CTCF	chr1:170324540-170324690	RPTEC	kidney:	n/a	n/a
38	CTCF	chr1:170344300-170344332	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr1:170406160-170406310	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr1:170384592-170384623	Lung_OC	lung:	n/a	n/a
41	CTCF	chr1:170406040-170406190	HVMF	connective:	n/a	n/a
42	CTCF	chr1:170406180-170406330	GM12873	blood:	n/a	n/a
43	CTCF	chr1:170316080-170316230	AG04449	skin:	n/a	n/a
44	CTCF	chr1:170353311-170353378	Medullo	brain:	n/a	n/a
45	CTCF	chr1:170406136-170406395	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr1:170324580-170324730	AG04449	skin:	n/a	n/a
47	CTCF	chr1:170338700-170338850	HMEC	breast:	n/a	n/a
48	CTCF	chr1:170316140-170316290	AG10803	skin:	n/a	n/a
49	CTCF	chr1:170324540-170324690	AG04449	skin:	n/a	n/a
50	CTCF	chr1:170406200-170406350	HMEC	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:170383965-170384015	SK-N-SH	brain:	n/a
2	chr1:170383965-170384015	SK-N-SH	brain:	n/a
3	chr1:170383965-170384015	HEK293	kidney:	embryo
4	chr1:170376975-170377025	SAEC	small airway:	n/a
5	chr1:170344621-170344671	NH-A	brain:	n/a
6	chr1:170383965-170384015	HEEpiC	esophagus:	n/a
7	chr1:170344621-170344671	MCF10A-Er-Src	breast:	n/a
8	chr1:170376975-170377025	AG09309	skin:	n/a
9	chr1:170376975-170377025	SKMC	muscle:	n/a
10	chr1:170376975-170377025	HMEC	breast:	n/a
11	chr1:170383965-170384015	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:170344621-170344671	AG09319	gingival:	n/a
13	chr1:170383965-170384015	IMR90	lung:	fetal
14	chr1:170344621-170344671	HUVEC	blood vessel:	n/a
15	chr1:170383965-170384015	BE2_C	brain:	n/a
16	chr1:170376975-170377025	NHBE	bronchial:	n/a
17	chr1:170376975-170377025	HUVEC	blood vessel:	n/a
18	chr1:170383965-170384015	T-47D	breast:	n/a
19	chr1:170344621-170344671	AG04450	lung:	fetal
20	chr1:170344621-170344671	SK-N-MC	brain:	n/a
21	chr1:170344621-170344671	SAEC	small airway:	n/a
22	chr1:170344621-170344671	SK-N-SH	brain:	n/a
23	chr1:170344621-170344671	K562	blood:	n/a
24	chr1:170383965-170384015	PANC-1	pancreas:	n/a
25	chr1:170383965-170384015	HUVEC	blood vessel:	n/a
26	chr1:170383965-170384015	Jurkat	blood:	n/a
27	chr1:170376975-170377025	IMR90	lung:	fetal
28	chr1:170376975-170377025	HAEpiC	amniotic membrane:	n/a
29	chr1:170383965-170384015	GM06990	blood:	n/a
30	chr1:170383965-170384015	CMK	blood:	n/a
31	chr1:170344621-170344671	H1-hESC	embryonic stem cell:	embryo
32	chr1:170383965-170384015	HIPEpiC	eye:	n/a
33	chr1:170383965-170384015	SK-N-SH_RA	brain:	n/a
34	chr1:170344621-170344671	Caco-2	colon:	n/a
35	chr1:170344621-170344671	U87	brain:	n/a
36	chr1:170383965-170384015	HCT-116	colon:	n/a
37	chr1:170383965-170384015	HCM	heart:	n/a
38	chr1:170376975-170377025	HCM	heart:	n/a
39	chr1:170376975-170377025	NH-A	brain:	n/a
40	chr1:170344621-170344671	NHBE	bronchial:	n/a
41	chr1:170344621-170344671	ProgFib	skin:	n/a
42	chr1:170383965-170384015	MCF10A-Er-Src	breast:	n/a
43	chr1:170376975-170377025	HEK293	kidney:	embryo
44	chr1:170383965-170384015	GM19239	blood:	n/a
45	chr1:170383965-170384015	HRCEpiC	kidney:	n/a
46	chr1:170344621-170344671	BE2_C	brain:	n/a
47	chr1:170383965-170384015	ovcar-3	ovarian:	n/a
48	chr1:170383965-170384015	AG09319	gingival:	n/a
49	chr1:170376975-170377025	GM06990	blood:	n/a
50	chr1:170376975-170377025	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:170406740..170408344-chr1:170500261..170502437,2	MCF-7	breast:
2	chr1:170321098..170321618-chr8:126444102..126444903,2	K562	blood:

No data

Variant related genes	Relation type
HAUS4P1	TF binding region
ENSG00000263384	TF binding region
HAUS4P1	CpG island
ENSG00000263384	CpG island
ENSG00000173334	chromatin interactions
ENSG00000231407	chromatin interactions
ENSG00000120370	chromatin interactions

Extended variants
information (count: 2022 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2022 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10494487	chr1:170315081-170315082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532296430	chr1:170315152-170315153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386636692	chr1:170315176-170315177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6660235	chr1:170315177-170315178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369658428	chr1:170315188-170315189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144325872	chr1:170315226-170315227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12407889	chr1:170315228-170315229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs561306399	chr1:170315308-170315309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147764812	chr1:170315309-170315310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570277040	chr1:170315361-170315362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549817279	chr1:170315377-170315378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539329398	chr1:170315378-170315379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187265114	chr1:170315400-170315401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538838403	chr1:170315425-170315426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547620013	chr1:170315431-170315432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189734035	chr1:170315435-170315436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536925709	chr1:170315469-170315470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113756811	chr1:170315564-170315565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180708100	chr1:170315606-170315607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571251504	chr1:170315614-170315615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146940425	chr1:170315695-170315696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147955533	chr1:170315744-170315745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538767379	chr1:170315752-170315753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577050803	chr1:170315787-170315788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs60073632	chr1:170315799-170315800	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs559615850	chr1:170316018-170316019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185054113	chr1:170316023-170316024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74992749	chr1:170316042-170316043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190300367	chr1:170316060-170316061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536026481	chr1:170316063-170316064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552923180	chr1:170316101-170316102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150527065	chr1:170316102-170316103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531729221	chr1:170316106-170316107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533740268	chr1:170316181-170316182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565022553	chr1:170316182-170316183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183195583	chr1:170316195-170316196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35456069	chr1:170316209-170316210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547509019	chr1:170316230-170316231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373938282	chr1:170316234-170316235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572499769	chr1:170316302-170316303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536456599	chr1:170316335-170316336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140604092	chr1:170316338-170316339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28545641	chr1:170316367-170316368	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs10753804	chr1:170316408-170316409	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs150444505	chr1:170316409-170316410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369313282	chr1:170316454-170316455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558243304	chr1:170316464-170316465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188425707	chr1:170316481-170316482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12091696	chr1:170316538-170316539	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs578037373	chr1:170316542-170316543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170312400-170319400	Weak transcription	Fetal Heart	heart
2	chr1:170315600-170316600	Enhancers	Dnd41	blood
3	chr1:170315800-170316800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:170316000-170316600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:170316600-170319400	Weak transcription	Dnd41	blood
6	chr1:170316600-170320200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:170316800-170320200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:170317600-170323400	Weak transcription	Pancreas	Pancrea
9	chr1:170319400-170320000	Enhancers	Dnd41	blood
10	chr1:170319400-170320600	Enhancers	Fetal Heart	heart
11	chr1:170320200-170321000	Enhancers	Right Atrium	heart
12	chr1:170320200-170321400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:170320200-170321600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:170320400-170320800	Enhancers	Left Ventricle	heart
15	chr1:170320400-170320800	Enhancers	Right Ventricle	heart
16	chr1:170320400-170321000	Enhancers	Aorta	Aorta
17	chr1:170320400-170321000	Enhancers	Psoas Muscle	Psoas
18	chr1:170320600-170323400	Weak transcription	Fetal Heart	heart
19	chr1:170320800-170323400	Weak transcription	Left Ventricle	heart
20	chr1:170321000-170321400	Weak transcription	Right Atrium	heart
21	chr1:170321000-170323400	Weak transcription	Psoas Muscle	Psoas
22	chr1:170321400-170321600	Enhancers	Right Atrium	heart
23	chr1:170321400-170323400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:170321600-170323400	Weak transcription	Right Atrium	heart
25	chr1:170323200-170324200	Enhancers	Fetal Intestine Large	intestine
26	chr1:170323400-170323600	Enhancers	Psoas Muscle	Psoas
27	chr1:170323400-170323800	Enhancers	Gastric	stomach
28	chr1:170323400-170323800	Enhancers	Left Ventricle	heart
29	chr1:170323400-170323800	Enhancers	Pancreas	Pancrea
30	chr1:170323400-170324000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:170323400-170324000	Enhancers	Right Atrium	heart
32	chr1:170323400-170325400	Enhancers	Fetal Heart	heart
33	chr1:170323600-170324000	Weak transcription	Psoas Muscle	Psoas
34	chr1:170326200-170326400	Enhancers	Psoas Muscle	Psoas
35	chr1:170336800-170337000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:170337200-170337400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:170338800-170339200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:170343800-170344600	Enhancers	Fetal Stomach	stomach
39	chr1:170343800-170346600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:170344000-170344400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:170344000-170344400	Enhancers	Lung	lung
42	chr1:170344000-170344600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr1:170344000-170345000	Enhancers	H9 Cell Line	embryonic stem cell
44	chr1:170344200-170345000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr1:170344600-170344800	Enhancers	NHLF	lung
46	chr1:170344600-170345000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr1:170344600-170345000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr1:170344600-170345200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr1:170344600-170345600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:170344600-170346400	Weak transcription	Fetal Stomach	stomach

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