Variant report

Variant	esv2757737
Chromosome Location	chr1:75986904-76187748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1543)
CpG islands
(count:1590)
Chromatin interactive
region (count:115)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1543 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76043585-76043706	K562	blood:	n/a	n/a
2	ARID3A	chr1:76143217-76143395	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:76082080-76082152	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:76105897-76106242	K562	blood:	n/a	n/a
5	ARID3A	chr1:75987556-75987697	K562	blood:	n/a	n/a
6	ARID3A	chr1:76172923-76173341	K562	blood:	n/a	n/a
7	ARID3A	chr1:76156263-76156463	K562	blood:	n/a	n/a
8	ARID3A	chr1:76138415-76138772	K562	blood:	n/a	n/a
9	ARID3A	chr1:76127609-76127665	K562	blood:	n/a	n/a
10	ARID3A	chr1:76142701-76143423	K562	blood:	n/a	n/a
11	ATF1	chr1:76109354-76109542	K562	blood:	n/a	n/a
12	ATF1	chr1:76105885-76106222	K562	blood:	n/a	n/a
13	ATF1	chr1:76080039-76080344	K562	blood:	n/a	n/a
14	ATF1	chr1:76172970-76173277	K562	blood:	n/a	n/a
15	ATF1	chr1:76156227-76156551	K562	blood:	n/a	n/a
16	ATF1	chr1:76139698-76139874	K562	blood:	n/a	n/a
17	ATF1	chr1:75986599-75986936	K562	blood:	n/a	n/a
18	ATF1	chr1:76082531-76082931	K562	blood:	n/a	n/a
19	ATF2	chr1:76095599-76095993	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr1:76138498-76138845	K562	blood:	n/a	n/a
21	BACH1	chr1:76137820-76137966	K562	blood:	n/a	n/a
22	BACH1	chr1:76137871-76139155	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:76003667-76003673	K562	blood:	n/a	n/a
24	BACH1	chr1:76082259-76082774	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr1:76138455-76138930	K562	blood:	n/a	n/a
26	BACH1	chr1:75994248-75994466	K562	blood:	n/a	n/a
27	BACH1	chr1:75986272-75986985	K562	blood:	n/a	n/a
28	BACH1	chr1:76080097-76080757	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr1:76049181-76049309	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL3	chr1:76050161-76050475	GM12878	blood:	n/a	n/a
31	BCLAF1	chr1:76172926-76173291	K562	blood:	n/a	n/a
32	BHLHE40	chr1:76105917-76106244	K562	blood:	n/a	n/a
33	BHLHE40	chr1:76186904-76187053	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:76107180-76107438	K562	blood:	n/a	n/a
35	BHLHE40	chr1:76047972-76048172	K562	blood:	n/a	n/a
36	BHLHE40	chr1:76049346-76049464	GM12878	blood:	n/a	n/a
37	BHLHE40	chr1:75993618-75993712	K562	blood:	n/a	n/a
38	BHLHE40	chr1:76007429-76007491	K562	blood:	n/a	n/a
39	BHLHE40	chr1:76082516-76082778	K562	blood:	n/a	n/a
40	BHLHE40	chr1:76137936-76138902	K562	blood:	n/a	n/a
41	BHLHE40	chr1:76098240-76098424	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:76172885-76173277	K562	blood:	n/a	n/a
43	BHLHE40	chr1:76105293-76105429	K562	blood:	n/a	n/a
44	BRCA1	chr1:76138437-76138629	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr1:76172998-76173358	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr1:76138277-76138932	K562	blood:	n/a	n/a
47	CBX3	chr1:76172760-76173391	K562	blood:	n/a	n/a
48	CBX3	chr1:76112759-76113226	K562	blood:	n/a	n/a
49	CCNT2	chr1:76081434-76081868	K562	blood:	n/a	n/a
50	CCNT2	chr1:76172904-76173197	K562	blood:	n/a	n/a

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76186078-76186128	Caco-2	colon:	n/a
2	chr1:76081962-76082012	HRPEpiC	eye:	n/a
3	chr1:76080727-76080777	T-47D	breast:	n/a
4	chr1:76076088-76076138	NB4	blood:	n/a
5	chr1:76186078-76186128	Caco-2	colon:	n/a
6	chr1:76081962-76082012	HRPEpiC	eye:	n/a
7	chr1:76080727-76080777	T-47D	breast:	n/a
8	chr1:76076088-76076138	NB4	blood:	n/a
9	chr1:76079177-76079227	NH-A	brain:	n/a
10	chr1:76080294-76080344	SAEC	small airway:	n/a
11	chr1:76079833-76079883	Hepatocyte	liver:	n/a
12	chr1:76080294-76080344	NHDF-neo	bronchial:	n/a
13	chr1:76082888-76082938	SK-N-SH_RA	brain:	n/a
14	chr1:76079833-76079883	CMK	blood:	n/a
15	chr1:76077832-76077882	A549	lung:	n/a
16	chr1:76082690-76082740	PFSK-1	brain:	n/a
17	chr1:76077832-76077882	GM19239	blood:	n/a
18	chr1:76078176-76078226	HRE	kidney:	n/a
19	chr1:76082690-76082740	GM12892	blood:	n/a
20	chr1:76082888-76082938	AG09319	gingival:	n/a
21	chr1:76080459-76080509	Caco-2	colon:	n/a
22	chr1:76080924-76080974	HMEC	breast:	n/a
23	chr1:76082690-76082740	HCF	heart:	n/a
24	chr1:76080684-76080734	NHBE	bronchial:	n/a
25	chr1:76080727-76080777	CMK	blood:	n/a
26	chr1:76138023-76138073	HCM	heart:	n/a
27	chr1:76080684-76080734	Hela-S3	cervix:	n/a
28	chr1:76079177-76079227	PrEC	prostate:	n/a
29	chr1:76186078-76186128	NHBE	bronchial:	n/a
30	chr1:76082690-76082740	BE2_C	brain:	n/a
31	chr1:76081962-76082012	LNCaP	prostate:	n/a
32	chr1:76082888-76082938	CMK	blood:	n/a
33	chr1:76095838-76095888	AG10803	skin:	n/a
34	chr1:76082173-76082223	U87	brain:	n/a
35	chr1:76186078-76186128	Hela-S3	cervix:	n/a
36	chr1:76138023-76138073	HCPEpiC	choroid plexus:	n/a
37	chr1:76138023-76138073	SAEC	small airway:	n/a
38	chr1:76077832-76077882	HIPEpiC	eye:	n/a
39	chr1:76080684-76080734	HCPEpiC	choroid plexus:	n/a
40	chr1:76186078-76186128	AG10803	skin:	n/a
41	chr1:76080924-76080974	NH-A	brain:	n/a
42	chr1:76085151-76085201	AG04450	lung:	fetal
43	chr1:76080684-76080734	HRPEpiC	eye:	n/a
44	chr1:76077832-76077882	HEEpiC	esophagus:	n/a
45	chr1:76079177-76079227	BJ	skin:	n/a
46	chr1:76079833-76079883	SAEC	small airway:	n/a
47	chr1:76082066-76082116	Hela-S3	cervix:	n/a
48	chr1:76078230-76078280	HRE	kidney:	n/a
49	chr1:76076088-76076138	Jurkat	blood:	n/a
50	chr1:76186078-76186128	RPTEC	kidney:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:76181545..76183225-chr1:76260845..76263669,2	K562	blood:
2	chr1:76070009..76076148-chr1:76078248..76081967,7	K562	blood:
3	chr1:76081387..76081887-chr15:39080643..39081147,2	Hela-S3	cervix:
4	chr1:76102793..76106233-chr1:76108594..76111145,3	K562	blood:
5	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
6	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
7	chr1:76083373..76085148-chr1:76086743..76089714,2	MCF-7	breast:
8	chr1:76138876..76140835-chr1:76251753..76254513,3	K562	blood:
9	chr1:76032378..76034524-chr1:76036114..76037930,2	K562	blood:
10	chr1:76079591..76081611-chr1:76189875..76191572,2	MCF-7	breast:
11	chr1:75985499..75987323-chr1:75988939..75991495,2	K562	blood:
12	chr1:76154691..76156608-chr1:76251098..76253830,2	K562	blood:
13	chr1:76096029..76098574-chr1:76101114..76103972,2	K562	blood:
14	chr1:76027597..76030890-chr1:76036483..76038711,3	K562	blood:
15	chr1:76071710..76074403-chr1:76079679..76081378,2	K562	blood:
16	chr1:75984267..75985784-chr1:76081741..76084002,2	K562	blood:
17	chr1:76031520..76033878-chr1:76036430..76038361,2	K562	blood:
18	chr1:76140961..76144068-chr1:76250261..76252961,3	K562	blood:
19	chr1:75731173..75731698-chr1:76097693..76098339,2	MCF-7	breast:
20	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
21	chr1:76152720..76155791-chr1:76253617..76257786,3	K562	blood:
22	chr1:76080604..76083289-chr1:76094142..76096069,2	K562	blood:
23	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
24	chr1:76153507..76155716-chr1:76158535..76161147,2	K562	blood:
25	chr1:76171478..76174682-chr1:76188816..76193676,7	K562	blood:
26	chr1:75985522..75987220-chr1:75991522..75993115,2	K562	blood:
27	chr1:76171242..76173918-chr1:76251777..76253452,2	MCF-7	breast:
28	chr1:76178176..76179962-chr1:76184780..76186701,2	K562	blood:
29	chr1:75993617..75995152-chr1:75995509..75998505,2	K562	blood:
30	chr1:76138718..76140997-chr1:76142345..76144918,2	K562	blood:
31	chr1:76027597..76030890-chr1:76036483..76038711,3	K562	blood:
32	chr1:76135960..76138598-chr1:76257398..76259099,2	K562	blood:
33	chr1:76081802..76083861-chr1:76085137..76086923,2	K562	blood:
34	chr1:76066835..76069254-chr1:76079406..76081859,2	MCF-7	breast:
35	chr1:76184568..76187287-chr1:76187578..76190885,3	MCF-7	breast:
36	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
37	chr1:76186306..76195796-chr1:76248732..76266552,73	K562	blood:
38	chr1:76031520..76033878-chr1:76036430..76038361,2	K562	blood:
39	chr1:75731104..75731714-chr1:76048302..76048818,2	K562	blood:
40	chr1:76070009..76076148-chr1:76078248..76081967,7	K562	blood:
41	chr1:76098237..76098781-chr1:76108716..76109281,2	K562	blood:
42	chr1:76032378..76034524-chr1:76036114..76037930,2	K562	blood:
43	chr1:76158085..76160004-chr1:76262153..76264534,2	K562	blood:
44	chr1:76178176..76179962-chr1:76184780..76186701,2	K562	blood:
45	chr1:75887927..75890320-chr1:76006872..76008474,2	K562	blood:
46	chr1:76160863..76164413-chr1:76188361..76190736,3	K562	blood:
47	chr1:76141089..76142781-chr1:76250261..76252071,2	K562	blood:
48	chr1:76079931..76081989-chr1:76083963..76086787,2	K562	blood:
49	chr1:76186929..76188557-chr16:30758246..30760309,2	K562	blood:
50	chr1:76168335..76170790-chr1:76173153..76175492,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC44A5-4	chr1:76105925-76108177	NONHSAT003984
2	lnc-SLC44A5-4	chr1:76186034-76186090	NONHSAT003984
3	lnc-SLC44A5-4	chr1:76175700-76176308	XLOC_000872
4	lnc-SLC44A5-4	chr1:76103852-76104725	NONHSAT003984
5	lnc-SLC44A5-4	chr1:76186030-76186090	XLOC_000872
6	lnc-SLC44A5-4	chr1:76175688-76176245	ENSG00000178193.5
7	lnc-ACADM-2	chr1:75987247-75987916	NONHSAT003981
8	lnc-SLC44A5-4	chr1:76107988-76108177	NONHSAT003985
9	lnc-SLC44A5-4	chr1:76186034-76186090	ENSG00000178193.5
10	lnc-SLC44A5-4	chr1:76143415-76143463	NONHSAT003985
11	lnc-SLC44A5-4	chr1:76174710-76174855	NONHSAT003984

No data

Variant related genes	Relation type
ACADM	TF binding region
SLC44A5	TF binding region
ENSG00000230863	TF binding region
ENSG00000213579	TF binding region
RNU6-503P	TF binding region
ENSG00000224493	TF binding region
ACADM	CpG island
SLC44A5	CpG island
ENSG00000230863	CpG island
ENSG00000213579	CpG island
RNU6-503P	CpG island
ENSG00000224493	CpG island
ENSG00000057468	chromatin interactions
ENSG00000207241	chromatin interactions
ENSG00000206620	chromatin interactions
ENSG00000117054	chromatin interactions
ENSG00000156873	chromatin interactions
ENSG00000178193	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000201487	chromatin interactions
ENSG00000224493	chromatin interactions
ENSG00000137955	chromatin interactions

Extended variants
information (count: 4583 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:4583 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72684153	chr1:75986999-75987000	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs1778451	chr1:75987001-75987002	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs567543541	chr1:75987044-75987045	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs372897647	chr1:75987069-75987070	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs112336279	chr1:75987076-75987077	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs534637629	chr1:75987111-75987112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114336596	chr1:75987132-75987133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571370950	chr1:75987191-75987192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183515763	chr1:75987256-75987257	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs556773962	chr1:75987293-75987294	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs575841390	chr1:75987352-75987353	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs536424216	chr1:75987361-75987362	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs372635835	chr1:75987387-75987388	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs112403421	chr1:75987418-75987419	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
15	rs564771851	chr1:75987465-75987466	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
16	rs1739902	chr1:75987470-75987471	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs140829240	chr1:75987527-75987528	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
18	rs200394425	chr1:75987549-75987550	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
19	rs564888429	chr1:75987658-75987659	Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs146645418	chr1:75987752-75987753	Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs77886525	chr1:75987759-75987760	Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs562835010	chr1:75987794-75987795	Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs78047966	chr1:75987868-75987869	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
24	rs548887897	chr1:75987959-75987960	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs373784748	chr1:75988001-75988002	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs372387992	chr1:75988004-75988005	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs550038971	chr1:75988035-75988036	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs561181096	chr1:75988042-75988043	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs74225850	chr1:75988043-75988044	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs115176713	chr1:75988044-75988045	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs2587034	chr1:75988045-75988046	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs78514352	chr1:75988054-75988055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs397689848	chr1:75988055-75988056	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs571307477	chr1:75988058-75988059	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs12402758	chr1:75988077-75988078	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs532012079	chr1:75988081-75988082	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs376956686	chr1:75988144-75988145	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs77646906	chr1:75988164-75988165	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs568844940	chr1:75988168-75988169	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs12402769	chr1:75988196-75988197	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs12067637	chr1:75988208-75988209	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs536868914	chr1:75988230-75988231	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs139096002	chr1:75988269-75988270	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs368603485	chr1:75988274-75988275	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs190812669	chr1:75988294-75988295	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs554715699	chr1:75988308-75988309	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs539968974	chr1:75988316-75988317	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs534181114	chr1:75988368-75988369	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs558814826	chr1:75988489-75988490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546254992	chr1:75988539-75988540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75983400-75987600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:75983600-75990200	Enhancers	Fetal Brain Male	brain
3	chr1:75985400-75987200	Enhancers	K562	blood
4	chr1:75985400-75988400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:75985800-75989000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr1:75986200-75987000	Enhancers	HepG2	liver
7	chr1:75986200-75987400	Enhancers	HUVEC	blood vessel
8	chr1:75986400-75987800	Enhancers	Fetal Brain Female	brain
9	chr1:75986600-75987000	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr1:75986600-75987800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:75986600-75988000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:75986600-75988000	Enhancers	NH-A	brain
13	chr1:75986800-75987600	Enhancers	Ovary	ovary
14	chr1:75987200-75988200	Weak transcription	K562	blood
15	chr1:75987400-75988400	Flanking Active TSS	HUVEC	blood vessel
16	chr1:75987400-75989000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:75987600-75987800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:75987800-75988200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:75987800-75988400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:75987800-75993400	Weak transcription	Fetal Brain Female	brain
21	chr1:75988200-75988600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:75988200-75988600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr1:75988200-75988600	Enhancers	K562	blood
24	chr1:75988400-75988600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:75988400-75989000	Enhancers	HUVEC	blood vessel
26	chr1:75988400-75998400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr1:75988600-75993200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:75989000-75993200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr1:75989000-75994400	Weak transcription	HUVEC	blood vessel
30	chr1:75990200-75994400	Weak transcription	Fetal Brain Male	brain
31	chr1:75993200-75994400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:75993200-75994400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:75993400-75993800	Enhancers	Adipose Nuclei	Adipose
34	chr1:75993400-75993800	Enhancers	K562	blood
35	chr1:75993400-75994800	Enhancers	Fetal Brain Female	brain
36	chr1:75993400-75995200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:75994400-75994800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr1:75994400-75995200	Enhancers	Fetal Brain Male	brain
39	chr1:75994400-75996000	Enhancers	HUVEC	blood vessel
40	chr1:75994400-75996200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:75995200-75996400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:75996000-75997000	Weak transcription	HUVEC	blood vessel
43	chr1:75996200-75997400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:75996400-75996800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr1:75996400-75997400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:75996600-75996800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:75997000-75997400	Enhancers	HUVEC	blood vessel
48	chr1:75997400-75998400	Weak transcription	HUVEC	blood vessel
49	chr1:75998400-75999400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:75998400-76000000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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