Variant report

Variant	esv3375162
Chromosome Location	chr1:179008554-179011102
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:35)
CpG islands
(count:123)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:35 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:179009122-179009189	K562	blood:	n/a	n/a
2	CBX3	chr1:179008970-179009459	K562	blood:	n/a	n/a
3	CEBPB	chr1:179008123-179008569	MCF-7	breast:	n/a	n/a
4	CUX1	chr1:179008582-179008898	K562	blood:	n/a	n/a
5	EP300	chr1:179007392-179008786	SK-N-SH	brain:	n/a	chr1:179008021-179008035 chr1:179007968-179007982
6	EP300	chr1:179009008-179009289	K562	blood:	n/a	n/a
7	GATA1	chr1:179007582-179009001	PBDE	blood:	n/a	chr1:179007844-179007853 chr1:179007840-179007856 chr1:179008292-179008301 chr1:179007726-179007737
8	GATA2	chr1:179008977-179009402	K562	blood:	n/a	n/a
9	GATA3	chr1:179007587-179008682	SK-N-SH	brain:	n/a	chr1:179007844-179007853 chr1:179007840-179007856 chr1:179008292-179008301 chr1:179007726-179007737
10	GATA3	chr1:179007565-179008579	SK-N-SH	brain:	n/a	chr1:179007844-179007853 chr1:179007840-179007856 chr1:179008292-179008301 chr1:179007726-179007737
11	GATA3	chr1:179007538-179008612	SH-SY5Y	brain:	n/a	chr1:179007844-179007853 chr1:179007840-179007856 chr1:179008292-179008301 chr1:179007726-179007737
12	KAP1	chr1:179007627-179008592	HEK293	kidney:	n/a	n/a
13	MAX	chr1:179008999-179009309	K562	blood:	n/a	n/a
14	MAX	chr1:179009090-179009311	K562	blood:	n/a	n/a
15	MAX	chr1:179009072-179009526	K562	blood:	n/a	n/a
16	MAZ	chr1:179009173-179009184	K562	blood:	n/a	n/a
17	MYC	chr1:179008983-179009366	K562	blood:	n/a	n/a
18	MYC	chr1:179009145-179009191	K562	blood:	n/a	n/a
19	MYC	chr1:179008996-179009522	K562	blood:	n/a	n/a
20	MYC	chr1:179008182-179008602	MCF10A-Er-Src	breast:	n/a	n/a
21	NR2F2	chr1:179008212-179009531	K562	blood:	n/a	n/a
22	NR2F2	chr1:179008851-179009336	K562	blood:	n/a	n/a
23	PML	chr1:179009043-179009462	K562	blood:	n/a	n/a
24	POLR2A	chr1:179009083-179009358	K562	blood:	n/a	n/a
25	POLR2A	chr1:179009154-179009235	K562	blood:	n/a	n/a
26	RCOR1	chr1:179009083-179009360	K562	blood:	n/a	n/a
27	STAT5A	chr1:179008987-179009342	K562	blood:	n/a	n/a
28	STAT5A	chr1:179008898-179009395	K562	blood:	n/a	n/a
29	TAL1	chr1:179008614-179009283	K562	blood:	n/a	n/a
30	TBL1XR1	chr1:179009173-179009180	K562	blood:	n/a	n/a
31	TEAD4	chr1:179009059-179009433	K562	blood:	n/a	n/a
32	TEAD4	chr1:179009068-179009358	K562	blood:	n/a	n/a
33	TRIM28	chr1:179008889-179009449	K562	blood:	n/a	n/a
34	YY1	chr1:179009175-179009449	K562	blood:	n/a	n/a
35	ZBTB7A	chr1:179009358-179009538	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179010239-179010289	HepG2	liver:	n/a
2	chr1:179010239-179010289	HepG2	liver:	n/a
3	chr1:179010239-179010289	AG09319	gingival:	n/a
4	chr1:179010239-179010289	PFSK-1	brain:	n/a
5	chr1:179010617-179010667	U87	brain:	n/a
6	chr1:179010239-179010289	HRE	kidney:	n/a
7	chr1:179010617-179010667	RPTEC	kidney:	n/a
8	chr1:179010617-179010667	A549	lung:	n/a
9	chr1:179010239-179010289	PrEC	prostate:	n/a
10	chr1:179010239-179010289	Hela-S3	cervix:	n/a
11	chr1:179010617-179010667	Caco-2	colon:	n/a
12	chr1:179010617-179010667	SKMC	muscle:	n/a
13	chr1:179010617-179010667	HCM	heart:	n/a
14	chr1:179010617-179010667	HCT-116	colon:	n/a
15	chr1:179010617-179010667	Hela-S3	cervix:	n/a
16	chr1:179010239-179010289	HRPEpiC	eye:	n/a
17	chr1:179010617-179010667	NB4	blood:	n/a
18	chr1:179010239-179010289	NB4	blood:	n/a
19	chr1:179010617-179010667	PFSK-1	brain:	n/a
20	chr1:179010239-179010289	GM12892	blood:	n/a
21	chr1:179010617-179010667	NT2-D1	testis:	n/a
22	chr1:179010617-179010667	NH-A	brain:	n/a
23	chr1:179010617-179010667	BJ	skin:	n/a
24	chr1:179010617-179010667	HRE	kidney:	n/a
25	chr1:179010239-179010289	AG04449	skin:	fetal
26	chr1:179010617-179010667	HAEpiC	amniotic membrane:	n/a
27	chr1:179010239-179010289	ovcar-3	ovarian:	n/a
28	chr1:179010617-179010667	HIPEpiC	eye:	n/a
29	chr1:179010617-179010667	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:179010617-179010667	SK-N-MC	brain:	n/a
31	chr1:179010239-179010289	GM12891	blood:	n/a
32	chr1:179010239-179010289	T-47D	breast:	n/a
33	chr1:179010617-179010667	HMEC	breast:	n/a
34	chr1:179010239-179010289	NT2-D1	testis:	n/a
35	chr1:179010239-179010289	A549	lung:	n/a
36	chr1:179010239-179010289	PANC-1	pancreas:	n/a
37	chr1:179010239-179010289	AG09309	skin:	n/a
38	chr1:179010239-179010289	HEEpiC	esophagus:	n/a
39	chr1:179010617-179010667	Hepatocyte	liver:	n/a
40	chr1:179010617-179010667	AG10803	skin:	n/a
41	chr1:179010617-179010667	AG04450	lung:	fetal
42	chr1:179010617-179010667	HL-60	blood:	n/a
43	chr1:179010239-179010289	LNCaP	prostate:	n/a
44	chr1:179010239-179010289	HCM	heart:	n/a
45	chr1:179010239-179010289	GM06990	blood:	n/a
46	chr1:179010617-179010667	HEEpiC	esophagus:	n/a
47	chr1:179010617-179010667	LNCaP	prostate:	n/a
48	chr1:179010239-179010289	HRCEpiC	kidney:	n/a
49	chr1:179010617-179010667	PANC-1	pancreas:	n/a
50	chr1:179010239-179010289	HUVEC	blood vessel:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179006880..179009225-chr1:179012117..179015129,3	MCF-7	breast:
2	chr1:179010945..179013494-chr1:179014600..179016271,4	K562	blood:
3	chr1:178993463..178996825-chr1:179010685..179014655,5	MCF-7	breast:
4	chr1:179008660..179014261-chr1:179016259..179020723,5	MCF-7	breast:
5	chr1:179006443..179009828-chr1:179013760..179016314,4	K562	blood:
6	chr1:178992800..178999926-chr1:179009509..179018222,23	K562	blood:
7	chr1:179006020..179008599-chr1:179014929..179016616,2	MCF-7	breast:
8	chr1:179008445..179010356-chr1:179011829..179013367,2	K562	blood:
9	chr1:179006443..179009675-chr1:179013601..179018312,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000232750	TF binding region
ENSG00000232750	CpG island
ENSG00000116199	chromatin interactions

Extended variants
information (count: 145 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:145 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533054141	chr1:179008652-179008653	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs537336387	chr1:179008678-179008679	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142145446	chr1:179008703-179008704	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs74385521	chr1:179008747-179008748	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs539081963	chr1:179008822-179008823	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs552996208	chr1:179008869-179008870	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs572833430	chr1:179008874-179008875	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200853125	chr1:179008876-179008877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs149898464	chr1:179008877-179008878	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs553458460	chr1:179008878-179008879	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs574731580	chr1:179008879-179008880	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs543666657	chr1:179008886-179008887	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs12064695	chr1:179008910-179008911	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs552684592	chr1:179008931-179008932	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs12064702	chr1:179008935-179008936	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs112027271	chr1:179008959-179008960	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545863871	chr1:179008971-179008972	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs559725019	chr1:179009012-179009013	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528594651	chr1:179009021-179009022	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs548743429	chr1:179009030-179009031	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs202038585	chr1:179009071-179009072	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs553652232	chr1:179009075-179009076	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs369307464	chr1:179009092-179009093	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs375509891	chr1:179009112-179009113	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs570668923	chr1:179009122-179009123	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs539751593	chr1:179009127-179009128	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs546254281	chr1:179009136-179009137	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs566175947	chr1:179009144-179009145	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs535168497	chr1:179009158-179009159	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs555051236	chr1:179009189-179009190	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs189183853	chr1:179009200-179009201	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs12068512	chr1:179009216-179009217	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs545580623	chr1:179009234-179009235	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs150403497	chr1:179009240-179009241	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs577446629	chr1:179009264-179009265	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs546522754	chr1:179009281-179009282	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181317084	chr1:179009288-179009289	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs376777603	chr1:179009296-179009297	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs542299020	chr1:179009303-179009304	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs562187431	chr1:179009317-179009318	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530687725	chr1:179009323-179009324	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs550484140	chr1:179009324-179009325	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564330642	chr1:179009343-179009344	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs533070803	chr1:179009348-179009349	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs546912244	chr1:179009362-179009363	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566090185	chr1:179009363-179009364	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs371315017	chr1:179009364-179009365	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs535084842	chr1:179009369-179009370	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs548638889	chr1:179009398-179009399	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs186505342	chr1:179009409-179009410	Weak transcription ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	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
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	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
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:178996200-179009200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:178996400-179011200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:178998200-179008600	Enhancers	Colon Smooth Muscle	Colon
4	chr1:178998400-179027400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:178999000-179009600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:179001200-179008600	Enhancers	Primary B cells from peripheral blood	blood
7	chr1:179001200-179009600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr1:179001600-179017000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr1:179001800-179008600	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr1:179001800-179016200	Weak transcription	Aorta	Aorta
11	chr1:179002000-179019200	Weak transcription	Adipose Nuclei	Adipose
12	chr1:179002800-179008600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr1:179003200-179008600	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr1:179003600-179009200	Weak transcription	Right Ventricle	heart
15	chr1:179003800-179011200	Weak transcription	Thymus	Thymus
16	chr1:179003800-179025800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr1:179004000-179011000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:179004200-179009200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr1:179004200-179010800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr1:179004200-179024200	Weak transcription	Liver	Liver
21	chr1:179004400-179012800	Weak transcription	Fetal Lung	lung
22	chr1:179004400-179013000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr1:179004400-179019200	Weak transcription	Duodenum Mucosa	Duodenum
24	chr1:179004400-179024200	Weak transcription	Fetal Kidney	kidney
25	chr1:179004800-179011200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr1:179004800-179012200	Weak transcription	Spleen	Spleen
27	chr1:179004800-179024600	Weak transcription	Primary B cells from cord blood	blood
28	chr1:179005000-179009000	Enhancers	K562	blood
29	chr1:179005200-179008600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr1:179005200-179008600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr1:179005200-179016400	Weak transcription	Left Ventricle	heart
32	chr1:179005400-179008600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr1:179005400-179008800	Enhancers	A549	lung
34	chr1:179005600-179008600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:179005600-179008800	Enhancers	Primary T cells from cord blood	blood
36	chr1:179005600-179008800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:179005600-179008800	Enhancers	Osteobl	bone
38	chr1:179005600-179009000	Enhancers	NHEK	skin
39	chr1:179005800-179008800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:179005800-179008800	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:179005800-179008800	Enhancers	HMEC	breast
42	chr1:179005800-179008800	Enhancers	HSMM	muscle
43	chr1:179005800-179009000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:179006000-179008600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr1:179006000-179008600	Enhancers	NHLF	lung
46	chr1:179006000-179024200	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:179006200-179008600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:179006200-179008800	Enhancers	HSMMtube	muscle
49	chr1:179006400-179008600	Enhancers	Hela-S3	cervix
50	chr1:179006400-179008800	Enhancers	GM12878-XiMat	blood

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