Variant report

Variant	esv3363004
Chromosome Location	chr1:217312379-217314377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:305)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:217313691-217313896	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr1:217313165-217313174	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD2	chr1:217313715-217314110	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr1:217312986-217314261	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTBP2	chr1:217311496-217312676	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F6	chr1:217313356-217314138	H1-hESC	embryonic stem cell:	n/a	chr1:217313597-217313609 chr1:217313559-217313568
7	E2F6	chr1:217313419-217314167	H1-hESC	embryonic stem cell:	n/a	chr1:217313597-217313609 chr1:217313559-217313568
8	GTF2F1	chr1:217313136-217313229	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAX	chr1:217313345-217313791	H1-hESC	embryonic stem cell:	n/a	chr1:217313746-217313756
10	MAX	chr1:217313374-217313835	H1-hESC	embryonic stem cell:	n/a	chr1:217313746-217313756
11	MAX	chr1:217313378-217314255	H1-hESC	embryonic stem cell:	n/a	chr1:217313746-217313756
12	MXI1	chr1:217313602-217313766	H1-hESC	embryonic stem cell:	n/a	n/a
13	MYC	chr1:217313247-217313714	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr1:217312589-217312604	MCF10A-Er-Src	breast:	n/a	n/a
15	POLR2A	chr1:217311416-217312468	H1-neurons	neurons:	n/a	n/a
16	POLR2A	chr1:217313335-217313858	H1-neurons	neurons:	n/a	n/a
17	POLR2A	chr1:217314066-217314533	H1-neurons	neurons:	n/a	n/a
18	POLR2A	chr1:217313217-217313787	H1-neurons	neurons:	n/a	n/a
19	POLR2A	chr1:217311387-217313261	H1-neurons	neurons:	n/a	n/a
20	RAD21	chr1:217313397-217313939	H1-hESC	embryonic stem cell:	n/a	n/a
21	SIN3A	chr1:217312969-217313169	H1-hESC	embryonic stem cell:	n/a	n/a
22	SIN3A	chr1:217313444-217313875	H1-hESC	embryonic stem cell:	n/a	n/a
23	SUZ12	chr1:217307066-217313271	NT2-D1	testis:	n/a	n/a
24	SUZ12	chr1:217309428-217313094	H1-hESC	embryonic stem cell:	n/a	n/a
25	TCF12	chr1:217313044-217313211	H1-hESC	embryonic stem cell:	n/a	n/a
26	YY1	chr1:217313758-217314342	H1-hESC	embryonic stem cell:	n/a	chr1:217314035-217314046
27	ZNF143	chr1:217313888-217314134	H1-hESC	embryonic stem cell:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:217312478-217312528	HRE	kidney:	n/a
2	chr1:217313044-217313094	SAEC	small airway:	n/a
3	chr1:217312478-217312528	BE2_C	brain:	n/a
4	chr1:217313699-217313749	NHDF-neo	bronchial:	n/a
5	chr1:217313824-217313874	NHDF-neo	bronchial:	n/a
6	chr1:217313699-217313749	A549	lung:	n/a
7	chr1:217314284-217314334	HMEC	breast:	n/a
8	chr1:217313699-217313749	H1-hESC	embryonic stem cell:	embryo
9	chr1:217313044-217313094	LNCaP	prostate:	n/a
10	chr1:217313699-217313749	Caco-2	colon:	n/a
11	chr1:217313824-217313874	HCM	heart:	n/a
12	chr1:217313824-217313874	Hepatocyte	liver:	n/a
13	chr1:217313699-217313749	Jurkat	blood:	n/a
14	chr1:217313044-217313094	MCF-7	breast:	n/a
15	chr1:217313044-217313094	NHBE	bronchial:	n/a
16	chr1:217313699-217313749	AG04450	lung:	fetal
17	chr1:217313824-217313874	HRPEpiC	eye:	n/a
18	chr1:217313044-217313094	AG09309	skin:	n/a
19	chr1:217314284-217314334	A549	lung:	n/a
20	chr1:217313824-217313874	U87	brain:	n/a
21	chr1:217312478-217312528	GM12891	blood:	n/a
22	chr1:217313824-217313874	NH-A	brain:	n/a
23	chr1:217313044-217313094	ovcar-3	ovarian:	n/a
24	chr1:217314284-217314334	RPTEC	kidney:	n/a
25	chr1:217314284-217314334	HAEpiC	amniotic membrane:	n/a
26	chr1:217313699-217313749	HEEpiC	esophagus:	n/a
27	chr1:217312478-217312528	BJ	skin:	n/a
28	chr1:217313044-217313094	H1-hESC	embryonic stem cell:	embryo
29	chr1:217313824-217313874	SK-N-SH	brain:	n/a
30	chr1:217313699-217313749	K562	blood:	n/a
31	chr1:217312478-217312528	HL-60	blood:	n/a
32	chr1:217313824-217313874	HCT-116	colon:	n/a
33	chr1:217313044-217313094	NHDF-neo	bronchial:	n/a
34	chr1:217313044-217313094	HEEpiC	esophagus:	n/a
35	chr1:217314284-217314334	HRE	kidney:	n/a
36	chr1:217313824-217313874	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:217313044-217313094	CMK	blood:	n/a
38	chr1:217314284-217314334	HRPEpiC	eye:	n/a
39	chr1:217312478-217312528	HRPEpiC	eye:	n/a
40	chr1:217313044-217313094	GM19239	blood:	n/a
41	chr1:217313699-217313749	AG09319	gingival:	n/a
42	chr1:217312478-217312528	HNPCEpiC	eye:	n/a
43	chr1:217313824-217313874	SAEC	small airway:	n/a
44	chr1:217313699-217313749	HCM	heart:	n/a
45	chr1:217312478-217312528	AG09319	gingival:	n/a
46	chr1:217313699-217313749	PANC-1	pancreas:	n/a
47	chr1:217312478-217312528	GM12878	blood:	n/a
48	chr1:217313699-217313749	CMK	blood:	n/a
49	chr1:217313699-217313749	ovcar-3	ovarian:	n/a
50	chr1:217313699-217313749	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:217311976..217314907-chr1:217319601..217322587,2	MCF-7	breast:
2	chr1:217308030..217310144-chr1:217311163..217313790,2	MCF-7	breast:

No data

Variant related genes	Relation type
ESRRG	TF binding region
ESRRG	CpG island

Extended variants
information (count: 82 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73104936	chr1:217312383-217312384	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141682706	chr1:217312453-217312454	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs544725120	chr1:217312454-217312455	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs558395776	chr1:217312462-217312463	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs575160982	chr1:217312481-217312482	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs543914262	chr1:217312505-217312506	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs201412982	chr1:217312567-217312568	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs201118685	chr1:217312568-217312569	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200036672	chr1:217312569-217312570	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs561625093	chr1:217312570-217312571	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs530420954	chr1:217312572-217312573	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs540789705	chr1:217312574-217312575	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs374346152	chr1:217312575-217312576	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs184245834	chr1:217312627-217312628	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532626532	chr1:217312735-217312736	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs552684557	chr1:217312742-217312743	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569289554	chr1:217312743-217312744	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs531726904	chr1:217312765-217312766	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs72743338	chr1:217312766-217312767	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs565546938	chr1:217312797-217312798	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs188565349	chr1:217312809-217312810	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536154423	chr1:217312816-217312817	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs552720714	chr1:217312850-217312851	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs150106164	chr1:217312904-217312905	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs538479295	chr1:217312935-217312936	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558610636	chr1:217312939-217312940	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs181063762	chr1:217313019-217313020	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544150324	chr1:217313024-217313025	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs527993363	chr1:217313025-217313026	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs374960093	chr1:217313044-217313045	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs185444927	chr1:217313054-217313055	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs368240338	chr1:217313061-217313062	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs575154025	chr1:217313105-217313106	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs12758982	chr1:217313112-217313113	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560796993	chr1:217313125-217313126	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs532739430	chr1:217313177-217313178	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs374485128	chr1:217313191-217313192	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs571233308	chr1:217313193-217313194	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs546125897	chr1:217313239-217313240	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs200622398	chr1:217313243-217313244	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs386639387	chr1:217313244-217313245	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs11591042	chr1:217313246-217313247	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs138410044	chr1:217313277-217313278	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs561767911	chr1:217313280-217313281	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs376477533	chr1:217313293-217313294	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs546472181	chr1:217313295-217313296	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs190970277	chr1:217313432-217313433	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs566469840	chr1:217313440-217313441	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs538445044	chr1:217313454-217313455	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs141511136	chr1:217313485-217313486	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Breast cancer	21858162	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217307200-217314200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
2	chr1:217307200-217314200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr1:217307400-217314200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
4	chr1:217309800-217312600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:217309800-217313800	Bivalent Enhancer	Fetal Brain Male	brain
6	chr1:217310000-217313000	Weak transcription	Right Atrium	heart
7	chr1:217311200-217313000	Weak transcription	Right Ventricle	heart
8	chr1:217311400-217312800	Bivalent Enhancer	Liver	Liver
9	chr1:217311400-217313200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
10	chr1:217311600-217312400	Bivalent Enhancer	Colonic Mucosa	Colon
11	chr1:217311800-217312400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:217311800-217312600	Weak transcription	Pancreas	Pancrea
13	chr1:217311800-217312800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
14	chr1:217311800-217312800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
15	chr1:217311800-217313000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:217311800-217313000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:217311800-217313200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
18	chr1:217312000-217312400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr1:217312000-217312400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
20	chr1:217312000-217312600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
21	chr1:217312000-217312600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr1:217312000-217312600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
23	chr1:217312000-217312600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:217312000-217312600	Bivalent/Poised TSS	NHEK	skin
25	chr1:217312000-217312800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:217312000-217312800	Enhancers	Brain Anterior Caudate	brain
27	chr1:217312000-217312800	Bivalent Enhancer	Fetal Kidney	kidney
28	chr1:217312000-217313000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr1:217312000-217313200	Bivalent Enhancer	Fetal Intestine Large	intestine
30	chr1:217312000-217313400	Bivalent Enhancer	Fetal Lung	lung
31	chr1:217312000-217313600	Bivalent Enhancer	Adipose Nuclei	Adipose
32	chr1:217312200-217312400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
33	chr1:217312200-217312600	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:217312200-217312800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:217312200-217312800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
36	chr1:217312400-217312600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
37	chr1:217312400-217312600	Bivalent Enhancer	Lung	lung
38	chr1:217312400-217312600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
39	chr1:217312400-217312800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:217312400-217312800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:217312400-217313600	Enhancers	Fetal Heart	heart
42	chr1:217312400-217313800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:217312400-217314000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr1:217312600-217312800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
45	chr1:217312600-217312800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
46	chr1:217312600-217312800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:217312600-217312800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
48	chr1:217312600-217312800	Enhancers	Pancreas	Pancrea
49	chr1:217312600-217312800	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
50	chr1:217312600-217312800	Bivalent Enhancer	NH-A	brain

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