Variant report

Variant	esv3452561
Chromosome Location	chr1:168339932-168343722
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	ARID3A	chr1:168343229-168343407	K562	blood:	n/a	n/a
2	ATF1	chr1:168341584-168341901	K562	blood:	n/a	n/a
3	ATF1	chr1:168343203-168343424	K562	blood:	n/a	n/a
4	ATF1	chr1:168342118-168342700	K562	blood:	n/a	n/a
5	ATF3	chr1:168343126-168343426	K562	blood:	n/a	n/a
6	BHLHE40	chr1:168343187-168343406	K562	blood:	n/a	n/a
7	BHLHE40	chr1:168341818-168342686	K562	blood:	n/a	n/a
8	CBX3	chr1:168341561-168342695	K562	blood:	n/a	n/a
9	CCNT2	chr1:168342245-168342534	K562	blood:	n/a	n/a
10	CCNT2	chr1:168343207-168343407	K562	blood:	n/a	n/a
11	CEBPB	chr1:168342049-168342676	K562	blood:	n/a	n/a
12	CEBPD	chr1:168342121-168342789	K562	blood:	n/a	n/a
13	CEBPD	chr1:168342091-168342677	K562	blood:	n/a	n/a
14	CUX1	chr1:168341620-168341821	K562	blood:	n/a	n/a
15	EGR1	chr1:168343177-168343459	K562	blood:	n/a	chr1:168343324-168343338 chr1:168343326-168343336 chr1:168343325-168343336 chr1:168343325-168343336 chr1:168343326-168343336
16	EGR1	chr1:168343179-168343491	K562	blood:	n/a	chr1:168343324-168343338 chr1:168343326-168343336 chr1:168343325-168343336 chr1:168343325-168343336 chr1:168343326-168343336
17	ELF1	chr1:168342107-168342741	K562	blood:	n/a	n/a
18	EP300	chr1:168341527-168341920	K562	blood:	n/a	n/a
19	EP300	chr1:168343205-168343460	K562	blood:	n/a	n/a
20	EP300	chr1:168342152-168342659	K562	blood:	n/a	n/a
21	EP300	chr1:168341637-168341793	K562	blood:	n/a	n/a
22	FOS	chr1:168343250-168343311	MCF10A-Er-Src	breast:	n/a	chr1:168343288-168343300 chr1:168343289-168343299 chr1:168343290-168343298 chr1:168343289-168343299
23	FOS	chr1:168343141-168343447	MCF10A-Er-Src	breast:	n/a	chr1:168343288-168343300 chr1:168343289-168343299 chr1:168343290-168343298 chr1:168343289-168343299
24	FOS	chr1:168343254-168343407	MCF10A-Er-Src	breast:	n/a	chr1:168343288-168343300 chr1:168343289-168343299 chr1:168343290-168343298 chr1:168343289-168343299
25	FOSL1	chr1:168343174-168343438	K562	blood:	n/a	chr1:168343288-168343300 chr1:168343288-168343299 chr1:168343289-168343299 chr1:168343290-168343298 chr1:168343289-168343299
26	FOSL1	chr1:168343153-168343439	K562	blood:	n/a	chr1:168343288-168343300 chr1:168343288-168343299 chr1:168343289-168343299 chr1:168343290-168343298 chr1:168343289-168343299
27	GATA1	chr1:168341490-168342781	PBDE	blood:	n/a	chr1:168341840-168341847 chr1:168342173-168342182
28	GATA1	chr1:168341967-168342851	K562	blood:	n/a	chr1:168342173-168342182
29	GATA2	chr1:168341499-168341958	K562	blood:	n/a	chr1:168341840-168341847
30	GATA2	chr1:168341595-168342635	K562	blood:	n/a	chr1:168341840-168341847 chr1:168342173-168342182
31	GATA2	chr1:168342114-168342645	K562	blood:	n/a	chr1:168342173-168342182
32	GTF2F1	chr1:168342414-168342613	K562	blood:	n/a	n/a
33	HDAC2	chr1:168343169-168343401	K562	blood:	n/a	n/a
34	HMGN3	chr1:168342197-168342843	K562	blood:	n/a	n/a
35	IRF1	chr1:168343201-168343380	K562	blood:	n/a	chr1:168343290-168343299
36	JUN	chr1:168341532-168342592	K562	blood:	n/a	chr1:168342175-168342183 chr1:168342173-168342185
37	JUN	chr1:168343153-168343449	K562	blood:	n/a	chr1:168343288-168343300 chr1:168343289-168343299 chr1:168343290-168343298 chr1:168343289-168343299
38	JUN	chr1:168343125-168343467	K562	blood:	n/a	chr1:168343288-168343300 chr1:168343289-168343299 chr1:168343290-168343298 chr1:168343289-168343299
39	JUND	chr1:168343121-168343491	K562	blood:	n/a	chr1:168343288-168343300 chr1:168343289-168343299 chr1:168343290-168343298 chr1:168343289-168343299
40	JUND	chr1:168341627-168342692	K562	blood:	n/a	chr1:168342175-168342183 chr1:168342173-168342185
41	MAFF	chr1:168343264-168343428	K562	blood:	n/a	n/a
42	MAFF	chr1:168342164-168342579	K562	blood:	n/a	n/a
43	MAFK	chr1:168343253-168343468	K562	blood:	n/a	n/a
44	MAFK	chr1:168342180-168342538	K562	blood:	n/a	n/a
45	MAX	chr1:168341560-168341952	K562	blood:	n/a	n/a
46	MAX	chr1:168341875-168342430	K562	blood:	n/a	chr1:168341961-168341970
47	MAX	chr1:168343111-168343386	K562	blood:	n/a	chr1:168343290-168343299
48	MAZ	chr1:168343209-168343449	K562	blood:	n/a	chr1:168343290-168343299
49	MAZ	chr1:168341620-168341843	K562	blood:	n/a	n/a
50	MYC	chr1:168341247-168341285	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:168343339-168343389	MCF10A-Er-Src	breast:	n/a
2	chr1:168343339-168343389	NHDF-neo	bronchial:	n/a
3	chr1:168343339-168343389	PFSK-1	brain:	n/a
4	chr1:168343339-168343389	NH-A	brain:	n/a
5	chr1:168343339-168343389	HAEpiC	amniotic membrane:	n/a
6	chr1:168343339-168343389	HCPEpiC	choroid plexus:	n/a
7	chr1:168343339-168343389	HepG2	liver:	n/a
8	chr1:168343339-168343389	AG09319	gingival:	n/a
9	chr1:168343339-168343389	AG04449	skin:	fetal
10	chr1:168343339-168343389	HCT-116	colon:	n/a
11	chr1:168343339-168343389	SAEC	small airway:	n/a
12	chr1:168343339-168343389	RPTEC	kidney:	n/a
13	chr1:168343339-168343389	HRCEpiC	kidney:	n/a
14	chr1:168343339-168343389	SKMC	muscle:	n/a
15	chr1:168343339-168343389	PANC-1	pancreas:	n/a
16	chr1:168343339-168343389	HRE	kidney:	n/a
17	chr1:168343339-168343389	GM12878	blood:	n/a
18	chr1:168343339-168343389	SK-N-SH	brain:	n/a
19	chr1:168343339-168343389	AoSMC	blood vessel:	n/a
20	chr1:168343339-168343389	H1-hESC	embryonic stem cell:	embryo
21	chr1:168343339-168343389	HCF	heart:	n/a
22	chr1:168343339-168343389	K562	blood:	n/a
23	chr1:168343339-168343389	T-47D	breast:	n/a
24	chr1:168343339-168343389	HEEpiC	esophagus:	n/a
25	chr1:168343339-168343389	Jurkat	blood:	n/a
26	chr1:168343339-168343389	NT2-D1	testis:	n/a
27	chr1:168343339-168343389	PrEC	prostate:	n/a
28	chr1:168343339-168343389	HEK293	kidney:	embryo
29	chr1:168343339-168343389	SK-N-SH_RA	brain:	n/a
30	chr1:168343339-168343389	AG10803	skin:	n/a
31	chr1:168343339-168343389	GM06990	blood:	n/a
32	chr1:168343339-168343389	GM19239	blood:	n/a
33	chr1:168343339-168343389	BJ	skin:	n/a
34	chr1:168343339-168343389	HNPCEpiC	eye:	n/a
35	chr1:168343339-168343389	IMR90	lung:	fetal
36	chr1:168343339-168343389	BE2_C	brain:	n/a
37	chr1:168343339-168343389	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:168343339-168343389	LNCaP	prostate:	n/a
39	chr1:168343339-168343389	HRPEpiC	eye:	n/a
40	chr1:168343339-168343389	ovcar-3	ovarian:	n/a
41	chr1:168343339-168343389	ProgFib	skin:	n/a
42	chr1:168343339-168343389	HIPEpiC	eye:	n/a
43	chr1:168343339-168343389	NHBE	bronchial:	n/a
44	chr1:168343339-168343389	GM12892	blood:	n/a
45	chr1:168343339-168343389	A549	lung:	n/a
46	chr1:168343339-168343389	HUVEC	blood vessel:	n/a
47	chr1:168343339-168343389	HCM	heart:	n/a
48	chr1:168343339-168343389	MCF-7	breast:	n/a
49	chr1:168343339-168343389	NB4	blood:	n/a
50	chr1:168343339-168343389	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:168338940..168340901-chr1:168341151..168343365,2	MCF-7	breast:
2	chr1:168338940..168340901-chr1:168341151..168343365,2	MCF-7	breast:
3	chr1:168342866..168344756-chr1:168372914..168374516,2	K562	blood:
4	chr1:168187433..168189118-chr1:168341371..168344286,2	K562	blood:
5	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:

Variant related genes	Relation type
MIR557	TF binding region
MIR557	CpG island

Extended variants
information (count: 154 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:154 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535390125	chr1:168339982-168339983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557312331	chr1:168339992-168339993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150259386	chr1:168340000-168340001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546008307	chr1:168340055-168340056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564124767	chr1:168340059-168340060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147879687	chr1:168340068-168340069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540383060	chr1:168340069-168340070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76110547	chr1:168340081-168340082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529271798	chr1:168340112-168340113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550528238	chr1:168340113-168340114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79495316	chr1:168340124-168340125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12726920	chr1:168340185-168340186	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs114356751	chr1:168340270-168340271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141537279	chr1:168340278-168340279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186757118	chr1:168340323-168340324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546378843	chr1:168340347-168340348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147075267	chr1:168340348-168340349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190263162	chr1:168340367-168340368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138373203	chr1:168340371-168340372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575659143	chr1:168340401-168340402	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs181765023	chr1:168340424-168340425	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539345502	chr1:168340466-168340467	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs73039775	chr1:168340473-168340474	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs572958675	chr1:168340477-168340478	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs540395492	chr1:168340534-168340535	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs555457088	chr1:168340535-168340536	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs368365739	chr1:168340537-168340538	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs186345288	chr1:168340543-168340544	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs149519385	chr1:168340554-168340555	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567757188	chr1:168340564-168340565	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs562538477	chr1:168340566-168340567	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs190994843	chr1:168340591-168340592	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs553470543	chr1:168340618-168340619	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs545385829	chr1:168340631-168340632	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs576736618	chr1:168340645-168340646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs560791648	chr1:168340679-168340680	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs182141715	chr1:168340748-168340749	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs186242510	chr1:168340775-168340776	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs116746754	chr1:168340788-168340789	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs143140452	chr1:168340818-168340819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550638320	chr1:168340836-168340837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73023403	chr1:168340840-168340841	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs539375575	chr1:168340846-168340847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191164212	chr1:168340893-168340894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148239517	chr1:168340919-168340920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533782790	chr1:168340969-168340970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555122677	chr1:168341040-168341041	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs573842537	chr1:168341044-168341045	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs544289145	chr1:168341085-168341086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2284760	chr1:168341108-168341109	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

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
Lung cancer	18438408	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
Myelofibrosis	22110671	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
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168331200-168341800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:168333200-168340800	Weak transcription	Right Atrium	heart
3	chr1:168336800-168341800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:168337200-168341600	Enhancers	K562	blood
5	chr1:168338000-168343000	Weak transcription	Aorta	Aorta
6	chr1:168338000-168343200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:168338200-168343400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:168338400-168348200	Weak transcription	HepG2	liver
9	chr1:168339400-168341400	Weak transcription	Placenta	Placenta
10	chr1:168339800-168340000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr1:168339800-168341000	Enhancers	Fetal Lung	lung
12	chr1:168340000-168341200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr1:168340200-168341400	Enhancers	Fetal Stomach	stomach
14	chr1:168340400-168340600	Enhancers	Right Ventricle	heart
15	chr1:168340400-168342200	Enhancers	Colon Smooth Muscle	Colon
16	chr1:168340400-168342200	Enhancers	Fetal Muscle Leg	muscle
17	chr1:168340600-168341200	Enhancers	Stomach Smooth Muscle	stomach
18	chr1:168340600-168341400	Weak transcription	Right Ventricle	heart
19	chr1:168340800-168342200	Enhancers	Rectal Smooth Muscle	rectum
20	chr1:168340800-168342600	Enhancers	Right Atrium	heart
21	chr1:168341000-168342000	Weak transcription	Fetal Lung	lung
22	chr1:168341200-168341400	Enhancers	Spleen	Spleen
23	chr1:168341200-168341600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr1:168341200-168342800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr1:168341400-168342200	Enhancers	Right Ventricle	heart
26	chr1:168341400-168342600	Enhancers	Placenta	Placenta
27	chr1:168341400-168342800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:168341600-168342000	Enhancers	Stomach Smooth Muscle	stomach
29	chr1:168341600-168342800	Enhancers	Fetal Heart	heart
30	chr1:168341600-168342800	Flanking Active TSS	K562	blood
31	chr1:168341800-168342200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr1:168341800-168342800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:168341800-168343400	Enhancers	Placenta Amnion	Placenta Amnion
34	chr1:168342000-168342200	Enhancers	Spleen	Spleen
35	chr1:168342000-168342400	Enhancers	Fetal Lung	lung
36	chr1:168342000-168342600	Enhancers	Left Ventricle	heart
37	chr1:168342000-168343400	Enhancers	Primary hematopoietic stem cells	blood
38	chr1:168342200-168343800	Weak transcription	Right Ventricle	heart
39	chr1:168342600-168343600	Weak transcription	Placenta	Placenta
40	chr1:168342600-168347400	Weak transcription	Right Atrium	heart
41	chr1:168342800-168345600	Enhancers	K562	blood
42	chr1:168343200-168343800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:168343600-168344800	Enhancers	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links