Variant report

Variant	esv1804634
Chromosome Location	chr1:225137134-225206826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225192292-225192433	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:225169624-225170034	HepG2	liver:	n/a	n/a
3	CBX3	chr1:225204354-225204636	K562	blood:	n/a	n/a
4	CBX3	chr1:225183306-225183672	HCT-116	colon:	n/a	n/a
5	CEBPB	chr1:225182531-225182863	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:225185901-225186263	HepG2	liver:	n/a	chr1:225186076-225186087
7	CEBPB	chr1:225185903-225186257	IMR90	lung:	n/a	chr1:225186076-225186087
8	CEBPB	chr1:225185918-225186199	MCF-7	breast:	n/a	chr1:225186076-225186087
9	CEBPB	chr1:225188410-225188431	HepG2	liver:	n/a	chr1:225188414-225188425
10	CEBPB	chr1:225144265-225144303	A549	lung:	n/a	n/a
11	CEBPB	chr1:225185883-225186203	ECC-1	luminal epithelium:	n/a	chr1:225186076-225186087
12	CEBPB	chr1:225185929-225186321	A549	lung:	n/a	chr1:225186076-225186087
13	CEBPB	chr1:225185911-225186272	K562	blood:	n/a	chr1:225186076-225186087
14	CEBPB	chr1:225185910-225186263	Hela-S3	cervix:	n/a	chr1:225186076-225186087
15	CEBPB	chr1:225188408-225188434	A549	lung:	n/a	chr1:225188414-225188425
16	CEBPB	chr1:225185945-225186230	H1-hESC	embryonic stem cell:	n/a	chr1:225186076-225186087
17	CEBPB	chr1:225182540-225182796	A549	lung:	n/a	n/a
18	CEBPB	chr1:225182674-225182786	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:225185938-225186201	A549	lung:	n/a	chr1:225186076-225186087
20	CEBPB	chr1:225185897-225186265	A549	lung:	n/a	chr1:225186076-225186087
21	CHD2	chr1:225169774-225169978	HepG2	liver:	n/a	n/a
22	CTCF	chr1:225192220-225192370	GM12873	blood:	n/a	n/a
23	CTCF	chr1:225192220-225192370	GM12865	blood:	n/a	n/a
24	CTCF	chr1:225192200-225192350	AG04450	lung:	n/a	n/a
25	CTCF	chr1:225192189-225192387	HepG2	liver:	n/a	n/a
26	CTCF	chr1:225192320-225192470	RPTEC	kidney:	n/a	n/a
27	CTCF	chr1:225192219-225192436	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:225192240-225192390	SAEC	small airway:	n/a	n/a
29	CTCF	chr1:225192260-225192410	HEK293	kidney:	n/a	n/a
30	CTCF	chr1:225192160-225192310	A549	lung:	n/a	n/a
31	CTCF	chr1:225192220-225192370	HCFaa	heart:	n/a	n/a
32	CTCF	chr1:225192280-225192430	AG10803	skin:	n/a	n/a
33	CTCF	chr1:225192260-225192410	GM12870	blood:	n/a	n/a
34	CTCF	chr1:225192320-225192470	HMEC	breast:	n/a	n/a
35	CTCF	chr1:225192220-225192370	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr1:225192360-225192510	HAc	cerebellar:	n/a	n/a
37	CTCF	chr1:225192200-225192350	NHEK	skin:	n/a	n/a
38	CTCF	chr1:225192240-225192390	GM12875	blood:	n/a	n/a
39	CTCF	chr1:225192240-225192390	HCT-116	colon:	n/a	n/a
40	CTCF	chr1:225192140-225192290	HL-60	blood:	n/a	n/a
41	CTCF	chr1:225192320-225192470	GM12872	blood:	n/a	n/a
42	CTCF	chr1:225192240-225192390	A549	lung:	n/a	n/a
43	CTCF	chr1:225192219-225192409	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr1:225192240-225192390	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr1:225192160-225192310	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr1:225192260-225192410	WI-38	lung:	n/a	n/a
47	CTCF	chr1:225192220-225192370	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr1:225192240-225192390	HMEC	breast:	n/a	n/a
49	CTCF	chr1:225192279-225192375	IMR90	lung:	n/a	n/a
50	CTCF	chr1:225192177-225192456	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225150341-225150391	NHDF-neo	bronchial:	n/a
2	chr1:225150341-225150391	PrEC	prostate:	n/a
3	chr1:225150341-225150391	SKMC	muscle:	n/a
4	chr1:225150341-225150391	HRPEpiC	eye:	n/a
5	chr1:225150341-225150391	RPTEC	kidney:	n/a
6	chr1:225150341-225150391	H1-hESC	embryonic stem cell:	embryo
7	chr1:225150341-225150391	HepG2	liver:	n/a
8	chr1:225150341-225150391	HRE	kidney:	n/a
9	chr1:225150341-225150391	GM06990	blood:	n/a
10	chr1:225150341-225150391	NH-A	brain:	n/a
11	chr1:225150341-225150391	HCPEpiC	choroid plexus:	n/a
12	chr1:225150341-225150391	MCF-7	breast:	n/a
13	chr1:225150341-225150391	HCM	heart:	n/a
14	chr1:225150341-225150391	AG09309	skin:	n/a
15	chr1:225150341-225150391	GM12892	blood:	n/a
16	chr1:225150341-225150391	GM12878	blood:	n/a
17	chr1:225150341-225150391	HRCEpiC	kidney:	n/a
18	chr1:225150341-225150391	HL-60	blood:	n/a
19	chr1:225150341-225150391	CMK	blood:	n/a
20	chr1:225150341-225150391	LNCaP	prostate:	n/a
21	chr1:225150341-225150391	AG04450	lung:	fetal
22	chr1:225150341-225150391	SK-N-SH_RA	brain:	n/a
23	chr1:225150341-225150391	HNPCEpiC	eye:	n/a
24	chr1:225150341-225150391	AoSMC	blood vessel:	n/a
25	chr1:225150341-225150391	ProgFib	skin:	n/a
26	chr1:225150341-225150391	HMEC	breast:	n/a
27	chr1:225150341-225150391	ovcar-3	ovarian:	n/a
28	chr1:225150341-225150391	MCF10A-Er-Src	breast:	n/a
29	chr1:225150341-225150391	AG10803	skin:	n/a
30	chr1:225150341-225150391	PFSK-1	brain:	n/a
31	chr1:225150341-225150391	Jurkat	blood:	n/a
32	chr1:225150341-225150391	HCF	heart:	n/a
33	chr1:225150341-225150391	HEEpiC	esophagus:	n/a
34	chr1:225150341-225150391	GM19239	blood:	n/a
35	chr1:225150341-225150391	AG04449	skin:	fetal
36	chr1:225150341-225150391	HCT-116	colon:	n/a
37	chr1:225150341-225150391	BE2_C	brain:	n/a
38	chr1:225150341-225150391	Caco-2	colon:	n/a
39	chr1:225150341-225150391	NHBE	bronchial:	n/a
40	chr1:225150341-225150391	Hela-S3	cervix:	n/a
41	chr1:225150341-225150391	K562	blood:	n/a
42	chr1:225150341-225150391	HAEpiC	amniotic membrane:	n/a
43	chr1:225150341-225150391	IMR90	lung:	fetal
44	chr1:225150341-225150391	NT2-D1	testis:	n/a
45	chr1:225150341-225150391	HEK293	kidney:	embryo
46	chr1:225150341-225150391	SK-N-SH	brain:	n/a
47	chr1:225150341-225150391	SAEC	small airway:	n/a
48	chr1:225150341-225150391	T-47D	breast:	n/a
49	chr1:225150341-225150391	BJ	skin:	n/a
50	chr1:225150341-225150391	NB4	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:225117272..225119612-chr1:225143482..225145459,3	K562	blood:
2	chr1:225138712..225141214-chr1:225147432..225149142,2	MCF-7	breast:
3	chr1:225133403..225135871-chr1:225146349..225149223,2	K562	blood:
4	chr1:225204703..225207335-chr1:225217608..225220449,2	K562	blood:
5	chr1:225151942..225154325-chr1:225156559..225160933,3	K562	blood:
6	chr1:225187463..225189933-chr1:225191453..225195155,3	K562	blood:
7	chr1:225148681..225151534-chr1:225153143..225154709,2	K562	blood:
8	chr1:225125254..225128428-chr1:225150698..225154229,3	K562	blood:
9	chr1:225187463..225189933-chr1:225191453..225195155,3	K562	blood:
10	chr1:225116223..225117951-chr1:225191253..225193259,2	MCF-7	breast:
11	chr1:225135426..225138299-chr1:225142390..225144172,2	MCF-7	breast:
12	chr1:225117272..225119024-chr1:225143959..225145501,2	K562	blood:
13	chr1:225148681..225151534-chr1:225153143..225154709,2	K562	blood:
14	chr1:225117903..225119549-chr1:225136065..225137999,2	K562	blood:
15	chr1:225133516..225138195-chr1:225140002..225143763,5	K562	blood:
16	chr1:225146634..225148217-chr1:225149675..225151960,2	K562	blood:
17	chr1:225151942..225154325-chr1:225156559..225160933,3	K562	blood:
18	chr1:225146634..225148217-chr1:225149675..225151960,2	K562	blood:
19	chr1:225202258..225204234-chr8:111898982..111900583,2	MCF-7	breast:
20	chr1:225117919..225119549-chr1:225136065..225138730,2	K562	blood:
21	chr1:225116575..225119201-chr1:225198743..225201718,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNIH3-4	chr1:225156461-225157195	NONHSAT009831
2	lnc-CNIH3-4	chr1:225155248-225155285	NONHSAT009831

No data

Variant related genes	Relation type
DNAH14	TF binding region
DNAH14	CpG island
ENSG00000185842	chromatin interactions

Extended variants
information (count: 2388 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2388 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2128268	chr1:225137134-225137135	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113643122	chr1:225137154-225137155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577738433	chr1:225137166-225137167	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1031995	chr1:225137246-225137247	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs369971990	chr1:225137299-225137300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs80229399	chr1:225137388-225137389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs145369553	chr1:225137462-225137463	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs368429161	chr1:225137527-225137528	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540608675	chr1:225137550-225137551	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs550342869	chr1:225137580-225137581	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562095547	chr1:225137587-225137588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529319147	chr1:225137590-225137591	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs16858661	chr1:225137627-225137628	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs569337277	chr1:225137628-225137629	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181018373	chr1:225137671-225137672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs551989990	chr1:225137672-225137673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs12738617	chr1:225137789-225137790	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs57850815	chr1:225137790-225137791	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553712891	chr1:225137844-225137845	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534249148	chr1:225137893-225137894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539183821	chr1:225137899-225137900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs79118182	chr1:225137921-225137922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566889860	chr1:225137975-225137976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186357516	chr1:225137986-225137987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555941242	chr1:225138035-225138036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577680276	chr1:225138060-225138061	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs544869479	chr1:225138100-225138101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553957423	chr1:225138111-225138112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs137856465	chr1:225138162-225138163	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572047392	chr1:225138179-225138180	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs115418860	chr1:225138224-225138225	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574034598	chr1:225138276-225138277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs4551561	chr1:225138350-225138351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544601509	chr1:225138366-225138367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562832518	chr1:225138373-225138374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191060531	chr1:225138395-225138396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182854125	chr1:225138401-225138402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560349162	chr1:225138459-225138460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552618348	chr1:225138504-225138505	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs572329645	chr1:225138505-225138506	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs2501066	chr1:225138553-225138554	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs61852099	chr1:225138566-225138567	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs200379853	chr1:225138574-225138575	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs75213215	chr1:225138575-225138576	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs554452040	chr1:225138585-225138586	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs369560398	chr1:225138629-225138630	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs537406247	chr1:225138669-225138670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2501065	chr1:225138697-225138698	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs571230877	chr1:225138758-225138759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544092503	chr1:225138759-225138760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
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
Breast cancer	17603634	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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Alzheimer''s disease	22166940	CNVD
micrognathia	21364285	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225133600-225156200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:225134200-225148600	Weak transcription	Pancreas	Pancrea
3	chr1:225135000-225146600	Weak transcription	HepG2	liver
4	chr1:225135200-225148600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr1:225136600-225145000	Weak transcription	K562	blood
6	chr1:225138200-225152800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:225138600-225155600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:225138800-225148600	Weak transcription	Fetal Intestine Large	intestine
9	chr1:225138800-225163800	Weak transcription	Hela-S3	cervix
10	chr1:225139200-225148600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:225139800-225148600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr1:225140000-225158400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr1:225140400-225140800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:225140600-225145000	Weak transcription	Liver	Liver
15	chr1:225141000-225142800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:225141000-225148600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:225141000-225149200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:225141200-225142800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:225141400-225158800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr1:225141400-225162600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr1:225141600-225159000	Weak transcription	Ovary	ovary
22	chr1:225141800-225159400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:225141800-225160200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr1:225142000-225143200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:225142000-225147800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:225142800-225143400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:225142800-225143600	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr1:225142800-225158400	Weak transcription	NH-A	brain
29	chr1:225142800-225162200	Weak transcription	Fetal Kidney	kidney
30	chr1:225142800-225164400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr1:225143200-225146400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:225143400-225151800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:225143400-225161800	Weak transcription	A549	lung
34	chr1:225143600-225145000	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr1:225145000-225145200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:225145000-225145600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr1:225145000-225145600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr1:225145000-225145600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:225145000-225145800	Strong transcription	Liver	Liver
40	chr1:225145000-225147000	Genic enhancers	K562	blood
41	chr1:225145200-225150200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr1:225145200-225160600	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr1:225145600-225152200	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr1:225145600-225158800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr1:225145800-225150000	Weak transcription	Liver	Liver
46	chr1:225146000-225147600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:225146400-225147600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:225146600-225147200	Enhancers	HepG2	liver
49	chr1:225147000-225157200	Strong transcription	K562	blood
50	chr1:225147200-225147400	Genic enhancers	HepG2	liver

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