Variant report

Variant	esv2762168
Chromosome Location	chr1:222717698-222736854
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:427)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:222729646-222730039	HepG2	liver:	n/a	n/a
2	ATF3	chr1:222720226-222720703	A549	lung:	n/a	n/a
3	ATF3	chr1:222720127-222720838	A549	lung:	n/a	n/a
4	BCL3	chr1:222720210-222721099	A549	lung:	n/a	n/a
5	BCL3	chr1:222720221-222720707	A549	lung:	n/a	n/a
6	CEBPB	chr1:222721668-222721952	IMR90	lung:	n/a	chr1:222721811-222721822 chr1:222721808-222721825
7	CEBPB	chr1:222731602-222731846	K562	blood:	n/a	chr1:222731678-222731689
8	CEBPB	chr1:222731554-222731845	IMR90	lung:	n/a	chr1:222731678-222731689
9	CEBPB	chr1:222720282-222720653	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:222731547-222731852	HepG2	liver:	n/a	chr1:222731678-222731689
11	CEBPB	chr1:222720098-222720837	A549	lung:	n/a	chr1:222720767-222720778
12	CEBPB	chr1:222720266-222720725	MCF-7	breast:	n/a	n/a
13	CEBPB	chr1:222720355-222720608	K562	blood:	n/a	n/a
14	CEBPB	chr1:222720235-222720664	A549	lung:	n/a	n/a
15	CEBPB	chr1:222720280-222720682	A549	lung:	n/a	n/a
16	CEBPB	chr1:222721740-222721907	K562	blood:	n/a	chr1:222721811-222721822 chr1:222721808-222721825
17	CEBPB	chr1:222725574-222725811	K562	blood:	n/a	n/a
18	CEBPB	chr1:222721636-222721988	HepG2	liver:	n/a	chr1:222721811-222721822 chr1:222721808-222721825
19	CEBPB	chr1:222731626-222731802	A549	lung:	n/a	chr1:222731678-222731689
20	CEBPB	chr1:222720211-222720734	MCF-7	breast:	n/a	n/a
21	CEBPB	chr1:222721639-222721974	A549	lung:	n/a	chr1:222721811-222721822 chr1:222721808-222721825
22	CEBPB	chr1:222720272-222720685	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:222720277-222720687	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:222729664-222730011	HepG2	liver:	n/a	n/a
25	CHD2	chr1:222720371-222720694	Hela-S3	cervix:	n/a	n/a
26	CREB1	chr1:222720474-222720795	A549	lung:	n/a	n/a
27	CTCF	chr1:222720500-222720650	HMF	breast:	n/a	n/a
28	CTCF	chr1:222720440-222720590	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr1:222720520-222720670	HCM	heart:	n/a	chr1:222720650-222720663
30	CTCF	chr1:222720539-222720597	Fibrobl	skin:	n/a	n/a
31	CTCF	chr1:222720500-222720650	SAEC	small airway:	n/a	n/a
32	CTCF	chr1:222726280-222726430	AG10803	skin:	n/a	n/a
33	CTCF	chr1:222735120-222735270	A549	lung:	n/a	n/a
34	CTCF	chr1:222735200-222735350	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr1:222720574-222720615	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr1:222735060-222735210	HMF	breast:	n/a	n/a
37	CTCF	chr1:222720500-222720650	HepG2	liver:	n/a	n/a
38	CTCF	chr1:222720460-222720610	HRE	kidney:	n/a	n/a
39	CTCF	chr1:222720500-222720650	NHEK	skin:	n/a	n/a
40	CTCF	chr1:222720460-222720610	AG10803	skin:	n/a	n/a
41	CTCF	chr1:222735040-222735190	HepG2	liver:	n/a	n/a
42	CTCF	chr1:222720540-222720690	AG04449	skin:	n/a	chr1:222720650-222720663
43	CTCF	chr1:222720480-222720630	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr1:222735160-222735310	BE2_C	brain:	n/a	n/a
45	CTCF	chr1:222735060-222735210	SAEC	small airway:	n/a	n/a
46	CTCF	chr1:222720640-222720790	SK-N-SH_RA	brain:	n/a	chr1:222720650-222720663
47	CTCF	chr1:222735120-222735410	NHEK	skin:	n/a	n/a
48	CTCF	chr1:222720300-222720450	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr1:222735100-222735250	HCT-116	colon:	n/a	n/a
50	CTCF	chr1:222720460-222720610	HCFaa	heart:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:222721375-222721425	LNCaP	prostate:	n/a
2	chr1:222721509-222721559	MCF10A-Er-Src	breast:	n/a
3	chr1:222721340-222721390	K562	blood:	n/a
4	chr1:222722210-222722260	AG09309	skin:	n/a
5	chr1:222722670-222722720	HRE	kidney:	n/a
6	chr1:222721375-222721425	H1-hESC	embryonic stem cell:	embryo
7	chr1:222721405-222721455	K562	blood:	n/a
8	chr1:222722210-222722260	Caco-2	colon:	n/a
9	chr1:222721509-222721559	PANC-1	pancreas:	n/a
10	chr1:222722495-222722545	HRCEpiC	kidney:	n/a
11	chr1:222722210-222722260	PANC-1	pancreas:	n/a
12	chr1:222721340-222721390	NHDF-neo	bronchial:	n/a
13	chr1:222722670-222722720	HEEpiC	esophagus:	n/a
14	chr1:222722210-222722260	MCF10A-Er-Src	breast:	n/a
15	chr1:222722495-222722545	K562	blood:	n/a
16	chr1:222722495-222722545	NHDF-neo	bronchial:	n/a
17	chr1:222721375-222721425	PrEC	prostate:	n/a
18	chr1:222722495-222722545	HEEpiC	esophagus:	n/a
19	chr1:222722495-222722545	T-47D	breast:	n/a
20	chr1:222721509-222721559	ECC-1	luminal epithelium:	n/a
21	chr1:222721509-222721559	HCT-116	colon:	n/a
22	chr1:222722210-222722260	NB4	blood:	n/a
23	chr1:222721375-222721425	HepG2	liver:	n/a
24	chr1:222721509-222721559	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:222721509-222721559	BJ	skin:	n/a
26	chr1:222721509-222721559	HUVEC	blood vessel:	n/a
27	chr1:222722210-222722260	SK-N-MC	brain:	n/a
28	chr1:222721509-222721559	K562	blood:	n/a
29	chr1:222721340-222721390	MCF10A-Er-Src	breast:	n/a
30	chr1:222721375-222721425	NB4	blood:	n/a
31	chr1:222721509-222721559	Hepatocyte	liver:	n/a
32	chr1:222722670-222722720	HCF	heart:	n/a
33	chr1:222721509-222721559	SK-N-SH	brain:	n/a
34	chr1:222722495-222722545	LNCaP	prostate:	n/a
35	chr1:222722495-222722545	HRE	kidney:	n/a
36	chr1:222722670-222722720	SK-N-MC	brain:	n/a
37	chr1:222721405-222721455	ovcar-3	ovarian:	n/a
38	chr1:222721405-222721455	BE2_C	brain:	n/a
39	chr1:222722210-222722260	GM06990	blood:	n/a
40	chr1:222722670-222722720	PANC-1	pancreas:	n/a
41	chr1:222721375-222721425	IMR90	lung:	fetal
42	chr1:222721340-222721390	HRPEpiC	eye:	n/a
43	chr1:222721375-222721425	BE2_C	brain:	n/a
44	chr1:222722670-222722720	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:222721375-222721425	GM19239	blood:	n/a
46	chr1:222722210-222722260	Jurkat	blood:	n/a
47	chr1:222721340-222721390	NHBE	bronchial:	n/a
48	chr1:222722495-222722545	HNPCEpiC	eye:	n/a
49	chr1:222722670-222722720	HUVEC	blood vessel:	n/a
50	chr1:222721405-222721455	AG04450	lung:	fetal

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:222720096..222721859-chr1:222816165..222817680,2	MCF-7	breast:
2	chr1:222735151..222737667-chr1:222771171..222774025,2	K562	blood:
3	chr1:222736167..222737997-chr1:222772404..222774025,2	K562	blood:
4	chr1:222719834..222721490-chr1:222725379..222727682,2	K562	blood:
5	chr1:222724484..222728107-chr1:222728855..222732774,4	K562	blood:
6	chr1:222725040..222727583-chr1:222792195..222794403,2	K562	blood:
7	chr1:222716628..222718719-chr1:222762257..222764765,2	MCF-7	breast:
8	chr1:222731468..222733360-chr1:222941211..222943133,2	K562	blood:
9	chr1:222736282..222738012-chr1:222762260..222764333,2	MCF-7	breast:
10	chr1:222736245..222737818-chr1:222743428..222745666,2	K562	blood:
11	chr1:222735227..222738969-chr1:222739039..222743402,4	K562	blood:
12	chr1:222723739..222728526-chr1:222728539..222731564,4	K562	blood:
13	chr1:222735935..222738524-chr1:222739039..222741294,2	K562	blood:
14	chr1:222718086..222720814-chr1:222790387..222793185,3	MCF-7	breast:
15	chr1:222731700..222734250-chr1:222758511..222761201,3	K562	blood:
16	chr1:222724484..222728107-chr1:222728855..222732774,4	K562	blood:
17	chr1:222723739..222728526-chr1:222728539..222731564,4	K562	blood:
18	chr1:222716769..222717818-chr1:222807560..222808441,6	MCF-7	breast:

No data

Variant related genes	Relation type
HHIPL2	TF binding region
HHIPL2	CpG island
ENSG00000143498	chromatin interactions
ENSG00000225265	chromatin interactions
ENSG00000143512	chromatin interactions
ENSG00000154305	chromatin interactions

Extended variants
information (count: 732 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17163185	chr1:222717698-222717699	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs17163186	chr1:222717788-222717789	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534011922	chr1:222717804-222717805	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs188546602	chr1:222717829-222717830	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs573944495	chr1:222717845-222717846	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538543638	chr1:222717852-222717853	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs140430444	chr1:222717894-222717895	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs193024526	chr1:222717931-222717932	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs67953393	chr1:222717958-222717959	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs545164675	chr1:222717968-222717969	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560299718	chr1:222718121-222718122	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs572632214	chr1:222718135-222718136	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs17509914	chr1:222718179-222718180	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs202190206	chr1:222718188-222718189	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs561732649	chr1:222718201-222718202	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs375833618	chr1:222718203-222718204	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs17163188	chr1:222718238-222718239	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs562736746	chr1:222718249-222718250	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs533247247	chr1:222718312-222718313	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs17463531	chr1:222718314-222718315	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs566664904	chr1:222718319-222718320	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs532080748	chr1:222718338-222718339	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs527823322	chr1:222718351-222718352	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs549171499	chr1:222718390-222718391	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs567657175	chr1:222718406-222718407	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs17463538	chr1:222718431-222718432	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557488267	chr1:222718443-222718444	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs556456629	chr1:222718490-222718491	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs373607977	chr1:222718519-222718520	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs538924995	chr1:222718586-222718587	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs79559306	chr1:222718600-222718601	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs145462803	chr1:222718632-222718633	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs185554699	chr1:222718644-222718645	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs555139731	chr1:222718645-222718646	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs36113683	chr1:222718674-222718675	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543899067	chr1:222718688-222718689	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs17011628	chr1:222718718-222718719	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs190515239	chr1:222718731-222718732	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs147689036	chr1:222718736-222718737	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560400874	chr1:222718773-222718774	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs527451116	chr1:222718804-222718805	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs192375245	chr1:222718884-222718885	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs567621878	chr1:222718892-222718893	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556906908	chr1:222718910-222718911	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549792574	chr1:222718944-222718945	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs571304603	chr1:222718977-222718978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs17463586	chr1:222719037-222719038	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
48	rs374561498	chr1:222719099-222719100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183740897	chr1:222719101-222719102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553997835	chr1:222719110-222719111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Congenital diaphragmatic hernia	21085971	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
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	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
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:222710200-222718600	Weak transcription	A549	lung
2	chr1:222713400-222720000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:222713600-222720000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:222714400-222718400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:222714400-222719400	Weak transcription	Osteobl	bone
6	chr1:222714400-222719600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:222715000-222718400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:222717200-222717800	Active TSS	HepG2	liver
9	chr1:222717400-222719600	Weak transcription	K562	blood
10	chr1:222717800-222718200	Weak transcription	HepG2	liver
11	chr1:222718400-222718600	Enhancers	HepG2	liver
12	chr1:222718400-222718600	Enhancers	NHDF-Ad	bronchial
13	chr1:222718400-222719400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:222718400-222719800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:222718400-222721000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:222718600-222718800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:222718600-222718800	Enhancers	A549	lung
18	chr1:222718600-222718800	Enhancers	HSMM	muscle
19	chr1:222718600-222719200	Weak transcription	HepG2	liver
20	chr1:222718600-222719200	Weak transcription	NHDF-Ad	bronchial
21	chr1:222718600-222719800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:222718800-222719000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr1:222718800-222719200	Weak transcription	A549	lung
24	chr1:222718800-222719600	Weak transcription	HSMM	muscle
25	chr1:222718800-222719800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr1:222718800-222720200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:222718800-222722000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:222719000-222719600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr1:222719200-222719600	Enhancers	A549	lung
30	chr1:222719200-222719800	Enhancers	NHDF-Ad	bronchial
31	chr1:222719200-222720200	Enhancers	HepG2	liver
32	chr1:222719400-222719600	Enhancers	Hela-S3	cervix
33	chr1:222719400-222719600	Enhancers	Osteobl	bone
34	chr1:222719400-222720000	Enhancers	HSMMtube	muscle
35	chr1:222719400-222721400	Enhancers	HMEC	breast
36	chr1:222719400-222721600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:222719400-222721600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:222719600-222719800	Flanking Active TSS	Hela-S3	cervix
39	chr1:222719600-222719800	Enhancers	HSMM	muscle
40	chr1:222719600-222719800	Enhancers	K562	blood
41	chr1:222719600-222720000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:222719600-222720000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:222719600-222720400	Enhancers	Fetal Kidney	kidney
44	chr1:222719600-222720400	Flanking Active TSS	A549	lung
45	chr1:222719600-222720800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:222719600-222721000	Enhancers	NH-A	brain
47	chr1:222719600-222721000	Flanking Active TSS	Osteobl	bone
48	chr1:222719600-222721200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr1:222719600-222721200	Enhancers	NHEK	skin
50	chr1:222719600-222721400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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