Variant report

Variant	esv1810844
Chromosome Location	chr1:246988018-247054824
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:500)
CpG islands
(count:122)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246990608-246991080	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:247046289-247046346	HepG2	liver:	n/a	n/a
3	ATF1	chr1:247000922-247001721	K562	blood:	n/a	n/a
4	ATF1	chr1:246996936-246997136	K562	blood:	n/a	n/a
5	ATF1	chr1:247020339-247020464	K562	blood:	n/a	n/a
6	ATF1	chr1:246988922-246989122	K562	blood:	n/a	n/a
7	ATF2	chr1:247000817-247001334	GM12878	blood:	n/a	n/a
8	BATF	chr1:247012945-247013122	GM12878	blood:	n/a	n/a
9	BATF	chr1:247038655-247039017	GM12878	blood:	n/a	chr1:247038791-247038802
10	BATF	chr1:247038587-247038975	GM12878	blood:	n/a	chr1:247038791-247038802
11	BCL3	chr1:247000857-247001417	A549	lung:	n/a	n/a
12	BCL3	chr1:247000955-247001559	GM12878	blood:	n/a	n/a
13	BCL3	chr1:247000855-247001613	K562	blood:	n/a	n/a
14	BCL3	chr1:246999639-247002277	A549	lung:	n/a	chr1:247001916-247001925
15	BCL3	chr1:247001751-247002512	K562	blood:	n/a	chr1:247001916-247001925
16	BCLAF1	chr1:247000975-247001507	GM12878	blood:	n/a	n/a
17	CBX3	chr1:246991970-246992630	K562	blood:	n/a	n/a
18	CBX3	chr1:246992103-246992482	K562	blood:	n/a	n/a
19	CBX3	chr1:246992107-246992622	HCT-116	colon:	n/a	n/a
20	CBX3	chr1:246992157-246992599	HCT-116	colon:	n/a	n/a
21	CCNT2	chr1:247000833-247001301	K562	blood:	n/a	n/a
22	CEBPB	chr1:247035337-247035635	HepG2	liver:	n/a	chr1:247035460-247035473 chr1:247035462-247035471 chr1:247035462-247035471 chr1:247035462-247035471
23	CEBPB	chr1:247020348-247020410	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:247035299-247035620	IMR90	lung:	n/a	chr1:247035460-247035473 chr1:247035462-247035471 chr1:247035462-247035471 chr1:247035462-247035471
25	CEBPB	chr1:247052395-247052595	HepG2	liver:	n/a	chr1:247052529-247052540
26	CEBPB	chr1:246998644-246998719	HepG2	liver:	n/a	chr1:246998663-246998674
27	CEBPB	chr1:247038452-247039314	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:247035313-247035627	K562	blood:	n/a	chr1:247035460-247035473 chr1:247035462-247035471 chr1:247035462-247035471 chr1:247035462-247035471
29	CEBPB	chr1:246999704-247000336	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:247052386-247052699	A549	lung:	n/a	chr1:247052529-247052540
31	CEBPB	chr1:247039001-247039290	A549	lung:	n/a	n/a
32	CHD2	chr1:247038870-247039087	GM12878	blood:	n/a	n/a
33	CHD2	chr1:247001060-247001225	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr1:247038860-247039010	AG04450	lung:	n/a	n/a
35	CTCF	chr1:247023445-247023529	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr1:247038720-247038870	BJ	skin:	n/a	n/a
37	CTCF	chr1:247002835-247002942	Lung_OC	lung:	n/a	n/a
38	CTCF	chr1:246997500-246997579	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr1:247001136-247001147	Fibrobl	skin:	n/a	n/a
40	CTCF	chr1:247038457-247038504	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:247002406-247002422	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr1:247051155-247051255	GM12878	blood:	n/a	chr1:247051172-247051193 chr1:247051170-247051188
43	CTCF	chr1:247051080-247051230	AG04450	lung:	n/a	chr1:247051172-247051193 chr1:247051170-247051188
44	CTCF	chr1:247015200-247015350	GM12875	blood:	n/a	n/a
45	CTCF	chr1:247013849-247013884	GM10266	blood:	n/a	n/a
46	CTCF	chr1:247051060-247051210	HPAF	blood vessel:	n/a	chr1:247051172-247051193 chr1:247051170-247051188
47	CTCF	chr1:247038900-247039050	AG04450	lung:	n/a	n/a
48	CTCF	chr1:247038860-247039010	AG04449	skin:	n/a	n/a
49	CTCF	chr1:247000800-247000950	K562	blood:	n/a	n/a
50	CTCF	chr1:247051040-247051190	HCPEpiC	choroid plexus:	n/a	chr1:247051170-247051188

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:247003430-247003480	AG04450	lung:	fetal
2	chr1:247003430-247003480	CMK	blood:	n/a
3	chr1:247003430-247003480	GM12892	blood:	n/a
4	chr1:247037632-247037682	IMR90	lung:	fetal
5	chr1:247003430-247003480	HUVEC	blood vessel:	n/a
6	chr1:247003430-247003480	HCM	heart:	n/a
7	chr1:247003430-247003480	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:247037632-247037682	AG04450	lung:	fetal
9	chr1:247003430-247003480	NHBE	bronchial:	n/a
10	chr1:247003430-247003480	HepG2	liver:	n/a
11	chr1:247037632-247037682	Hela-S3	cervix:	n/a
12	chr1:247037632-247037682	HCPEpiC	choroid plexus:	n/a
13	chr1:247037632-247037682	Jurkat	blood:	n/a
14	chr1:247003430-247003480	HEEpiC	esophagus:	n/a
15	chr1:247003430-247003480	K562	blood:	n/a
16	chr1:247037632-247037682	ovcar-3	ovarian:	n/a
17	chr1:247003430-247003480	AG10803	skin:	n/a
18	chr1:247003430-247003480	Caco-2	colon:	n/a
19	chr1:247037632-247037682	Hepatocyte	liver:	n/a
20	chr1:247037632-247037682	MCF-7	breast:	n/a
21	chr1:247037632-247037682	AG09309	skin:	n/a
22	chr1:247003430-247003480	AG04449	skin:	fetal
23	chr1:247037632-247037682	HNPCEpiC	eye:	n/a
24	chr1:247037632-247037682	RPTEC	kidney:	n/a
25	chr1:247037632-247037682	SK-N-SH_RA	brain:	n/a
26	chr1:247037632-247037682	T-47D	breast:	n/a
27	chr1:247037632-247037682	AoSMC	blood vessel:	n/a
28	chr1:247003430-247003480	HRPEpiC	eye:	n/a
29	chr1:247003430-247003480	NT2-D1	testis:	n/a
30	chr1:247037632-247037682	A549	lung:	n/a
31	chr1:247003430-247003480	A549	lung:	n/a
32	chr1:247037632-247037682	NHBE	bronchial:	n/a
33	chr1:247003430-247003480	PrEC	prostate:	n/a
34	chr1:247003430-247003480	GM06990	blood:	n/a
35	chr1:247037632-247037682	SKMC	muscle:	n/a
36	chr1:247037632-247037682	BJ	skin:	n/a
37	chr1:247003430-247003480	AG09309	skin:	n/a
38	chr1:247003430-247003480	AoSMC	blood vessel:	n/a
39	chr1:247037632-247037682	NB4	blood:	n/a
40	chr1:247003430-247003480	LNCaP	prostate:	n/a
41	chr1:247037632-247037682	HCT-116	colon:	n/a
42	chr1:247037632-247037682	GM12878	blood:	n/a
43	chr1:247003430-247003480	Jurkat	blood:	n/a
44	chr1:247037632-247037682	GM12892	blood:	n/a
45	chr1:247003430-247003480	HNPCEpiC	eye:	n/a
46	chr1:247037632-247037682	U87	brain:	n/a
47	chr1:247037632-247037682	HRE	kidney:	n/a
48	chr1:247003430-247003480	HMEC	breast:	n/a
49	chr1:247037632-247037682	GM19239	blood:	n/a
50	chr1:247003430-247003480	T-47D	breast:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:247000376..247002302-chr1:247040440..247042162,2	K562	blood:
2	chr1:247017685..247021797-chr1:247033247..247038806,7	K562	blood:
3	chr1:247019729..247021286-chr1:247026744..247028354,2	K562	blood:
4	chr1:247030642..247032624-chr1:247035866..247038095,2	K562	blood:
5	chr1:247039071..247040788-chr1:247042685..247044930,2	K562	blood:
6	chr1:247030122..247032370-chr1:247032584..247035559,2	K562	blood:
7	chr1:247017312..247021045-chr1:247051011..247055284,3	K562	blood:
8	chr1:247028600..247030122-chr1:247031520..247034371,2	K562	blood:
9	chr1:247041147..247045524-chr1:247051435..247055344,4	K562	blood:
10	chr1:247000678..247002401-chr1:247004834..247006838,2	K562	blood:
11	chr1:246996938..246999359-chr1:247044207..247046740,2	K562	blood:
12	chr1:247033154..247036008-chr1:247106994..247108758,2	MCF-7	breast:
13	chr1:247028600..247030122-chr1:247031520..247034371,2	K562	blood:
14	chr1:246999464..247001183-chr1:247004017..247007456,3	MCF-7	breast:
15	chr1:247017312..247021045-chr1:247051011..247055284,3	K562	blood:
16	chr1:247000678..247002401-chr1:247004834..247006838,2	K562	blood:
17	chr1:247051414..247053728-chr1:247080520..247082221,2	K562	blood:
18	chr1:246999464..247001183-chr1:247004017..247007456,3	MCF-7	breast:
19	chr1:247046300..247048217-chr1:247091357..247094558,3	K562	blood:
20	chr1:246822078..246824863-chr1:247030582..247033303,2	K562	blood:
21	chr1:247053879..247054578-chr11:118965786..118966471,2	NB4	blood:
22	chr1:247000376..247002302-chr1:247040440..247042162,2	K562	blood:
23	chr1:247019583..247021599-chr1:247036719..247038806,2	K562	blood:
24	chr1:247049317..247052263-chr1:247093673..247095503,2	K562	blood:
25	chr1:247030122..247032370-chr1:247032584..247035559,2	K562	blood:
26	chr1:247015867..247018151-chr1:247054871..247056907,2	K562	blood:
27	chr1:247014087..247017239-chr1:247019400..247022129,3	K562	blood:
28	chr1:246991725..246994648-chr1:247001780..247004599,2	K562	blood:
29	chr1:247001934..247004833-chr1:247007258..247009999,3	K562	blood:
30	chr1:247012591..247014544-chr1:247016380..247018408,3	K562	blood:
31	chr1:246996938..246999359-chr1:247044207..247046740,2	K562	blood:
32	chr1:247001934..247004833-chr1:247007258..247009999,3	K562	blood:
33	chr1:247017685..247021797-chr1:247033247..247038806,7	K562	blood:
34	chr1:247019583..247021599-chr1:247036719..247038806,2	K562	blood:
35	chr1:247014087..247017239-chr1:247019400..247022129,3	K562	blood:
36	chr1:247041147..247045524-chr1:247051435..247055344,4	K562	blood:
37	chr1:247053838..247055850-chr1:247057759..247060432,2	K562	blood:
38	chr1:247005474..247007845-chr1:247009959..247011844,2	K562	blood:
39	chr1:247005474..247007845-chr1:247009959..247011844,2	K562	blood:
40	chr1:247030642..247032624-chr1:247035866..247038095,2	K562	blood:
41	chr1:246986424..246989892-chr1:246990442..246996940,6	K562	blood:
42	chr1:247029799..247031525-chr1:247058523..247060785,2	MCF-7	breast:
43	chr1:247027725..247030371-chr1:247093774..247095818,2	MCF-7	breast:
44	chr1:247026865..247028618-chr1:247028960..247030926,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-439E19.8.1-2	chr1:247027226-247027600	NONHSAT010745
2	lnc-RP11-439E19.8.1-2	chr1:247025260-247025455	NONHSAT010745

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AHCTF1	hsa-let-7b-5p	chr1:247003548-247003541
2	AHCTF1	hsa-let-7b-5p	chr1:247003542-247003563

Variant related genes	Relation type
KIF28P	TF binding region
ENSG00000252011	TF binding region
AHCTF1	TF binding region
KIF28P	CpG island
ENSG00000252011	CpG island
AHCTF1	CpG island
ENSG00000223519	chromatin interactions
ENSG00000153207	chromatin interactions
ENSG00000252011	chromatin interactions
ENSG00000188486	chromatin interactions

Extended variants
information (count: 2930 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2930 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552456618	chr1:246988092-246988093	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs562894477	chr1:246988098-246988099	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs56703524	chr1:246988168-246988169	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531876705	chr1:246988175-246988176	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs12038733	chr1:246988179-246988180	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs556627697	chr1:246988191-246988192	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568618691	chr1:246988193-246988194	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557739538	chr1:246988194-246988195	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs190528979	chr1:246988200-246988201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534056495	chr1:246988206-246988207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376565870	chr1:246988213-246988214	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs76207307	chr1:246988293-246988294	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570869071	chr1:246988303-246988304	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs193269985	chr1:246988313-246988314	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs556593712	chr1:246988399-246988400	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112218980	chr1:246988454-246988455	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs184245835	chr1:246988486-246988487	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs535722566	chr1:246988503-246988504	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs188958148	chr1:246988576-246988577	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs202198308	chr1:246988585-246988586	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs572174468	chr1:246988613-246988614	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs143109397	chr1:246988614-246988615	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs118161765	chr1:246988673-246988674	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs150826252	chr1:246988675-246988676	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543056530	chr1:246988790-246988791	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs181063643	chr1:246988797-246988798	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs72190919	chr1:246988800-246988801	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs78461062	chr1:246988805-246988806	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531910774	chr1:246988810-246988811	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs542482230	chr1:246988811-246988812	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148848312	chr1:246988812-246988813	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113889555	chr1:246988813-246988814	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs111559170	chr1:246988814-246988815	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112342362	chr1:246988815-246988816	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs78759581	chr1:246988819-246988820	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111365553	chr1:246988823-246988824	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs185641391	chr1:246988825-246988826	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs189433638	chr1:246988841-246988842	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs559097786	chr1:246988886-246988887	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs374782296	chr1:246988918-246988919	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs538426300	chr1:246988922-246988923	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs371681895	chr1:246988925-246988926	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568768429	chr1:246988926-246988927	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547577002	chr1:246988937-246988938	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs200184066	chr1:246988938-246988939	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs113716958	chr1:246988939-246988940	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527561117	chr1:246988940-246988941	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs369474325	chr1:246988945-246988946	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539893777	chr1:246988946-246988947	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs79373579	chr1:246988947-246988948	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	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
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1538 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246981400-246989000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:246986400-246992200	Weak transcription	Brain Substantia Nigra	brain
3	chr1:246987800-246988600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:246988800-246989200	ZNF genes & repeats	Fetal Kidney	kidney
5	chr1:246989000-246989400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:246989200-247011200	Weak transcription	Fetal Kidney	kidney
7	chr1:246990000-246991200	Enhancers	HepG2	liver
8	chr1:246990600-246990800	Enhancers	Hela-S3	cervix
9	chr1:246990800-246991200	Flanking Active TSS	Hela-S3	cervix
10	chr1:246990800-246991200	Enhancers	NHEK	skin
11	chr1:246993200-247004200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr1:246994600-246994800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr1:246994800-246995000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:246994800-246995000	Enhancers	HUVEC	blood vessel
15	chr1:246994800-246995200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:246994800-246995200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:246994800-247003200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr1:246995000-246995400	Flanking Active TSS	HUVEC	blood vessel
19	chr1:246995200-246996800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:246995200-246996800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:246995200-247001400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:246995400-247004200	Weak transcription	HUVEC	blood vessel
23	chr1:246996600-246997400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr1:246996800-246997000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr1:246996800-246997800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:246996800-246997800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:246996800-246999000	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr1:246997000-246997400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr1:246997000-246997800	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr1:246997400-246999600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr1:246997400-247002200	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr1:246997800-246998200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:246997800-246998200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:246997800-246999600	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr1:246998200-246999000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:246998200-246999200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:246998600-246998800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr1:246998800-247004200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr1:246999000-246999200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:246999000-246999200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr1:246999000-246999400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:246999000-246999800	Enhancers	Ovary	ovary
43	chr1:246999000-247002400	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr1:246999200-246999600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:246999200-247004600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr1:246999200-247010000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:246999400-247001200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:246999400-247004000	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr1:246999400-247004200	Weak transcription	Stomach Smooth Muscle	stomach
50	chr1:246999600-246999800	Enhancers	Muscle Satellite Cultured Cells	--

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