Variant report

Variant	esv1826403
Chromosome Location	chr3:47912703-48012797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:540)
CpG islands
(count:488)
Chromatin interactive
region (count:45)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:48003444-48004114	K562	blood:	n/a	n/a
2	ARID3A	chr3:48006096-48006657	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:47991572-47992014	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:47952454-47952470	K562	blood:	n/a	n/a
5	ARID3A	chr3:47912920-47913184	K562	blood:	n/a	n/a
6	ARID3A	chr3:47995961-47996755	HepG2	liver:	n/a	n/a
7	ATF1	chr3:47914032-47914186	K562	blood:	n/a	n/a
8	ATF1	chr3:47912838-47913288	K562	blood:	n/a	n/a
9	BACH1	chr3:48003559-48003759	K562	blood:	n/a	n/a
10	BACH1	chr3:47952257-47952646	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:47951220-47951243	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:47952274-47952594	K562	blood:	n/a	n/a
13	BCLAF1	chr3:47984762-47985166	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:47914856-47914863	A549	lung:	n/a	n/a
15	BHLHE40	chr3:47991948-47992285	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:48005785-48005906	K562	blood:	n/a	n/a
17	BHLHE40	chr3:48003402-48003990	K562	blood:	n/a	n/a
18	BHLHE40	chr3:47912915-47913276	K562	blood:	n/a	n/a
19	BRCA1	chr3:47991218-47991257	GM12878	blood:	n/a	n/a
20	CBX3	chr3:48003163-48003744	K562	blood:	n/a	n/a
21	CBX3	chr3:47912466-47913365	K562	blood:	n/a	n/a
22	CCNT2	chr3:47914670-47914690	K562	blood:	n/a	n/a
23	CCNT2	chr3:48003822-48004364	K562	blood:	n/a	n/a
24	CEBPB	chr3:48006264-48006557	IMR90	lung:	n/a	chr3:48006478-48006489
25	CEBPB	chr3:47942799-47943145	HepG2	liver:	n/a	chr3:47942971-47942982
26	CEBPB	chr3:47979849-47980073	K562	blood:	n/a	chr3:47979919-47979930
27	CEBPB	chr3:47952212-47952595	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr3:47942851-47943099	HepG2	liver:	n/a	chr3:47942971-47942982
29	CEBPB	chr3:48006175-48006588	K562	blood:	n/a	chr3:48006182-48006195 chr3:48006478-48006489
30	CEBPB	chr3:47935519-47935646	K562	blood:	n/a	n/a
31	CEBPB	chr3:47970716-47970887	HepG2	liver:	n/a	chr3:47970796-47970807
32	CEBPB	chr3:47931924-47932402	H1-hESC	embryonic stem cell:	n/a	chr3:47932017-47932028 chr3:47932018-47932027 chr3:47932016-47932027
33	CEBPB	chr3:47979865-47980069	HepG2	liver:	n/a	chr3:47979919-47979930
34	CEBPB	chr3:47970760-47970876	Hela-S3	cervix:	n/a	chr3:47970796-47970807
35	CEBPB	chr3:48003759-48004013	K562	blood:	n/a	n/a
36	CEBPB	chr3:47974719-47974888	HepG2	liver:	n/a	chr3:47974804-47974815
37	CEBPB	chr3:47931844-47932195	K562	blood:	n/a	chr3:47932017-47932028 chr3:47932018-47932027 chr3:47932016-47932027
38	CEBPB	chr3:47973952-47974237	IMR90	lung:	n/a	n/a
39	CEBPB	chr3:47931933-47932165	HepG2	liver:	n/a	chr3:47932017-47932028 chr3:47932018-47932027 chr3:47932016-47932027
40	CEBPB	chr3:48006273-48006662	HepG2	liver:	n/a	chr3:48006478-48006489
41	CEBPB	chr3:48006266-48006522	H1-hESC	embryonic stem cell:	n/a	chr3:48006478-48006489
42	CEBPB	chr3:48006277-48006541	A549	lung:	n/a	chr3:48006478-48006489
43	CEBPB	chr3:47931885-47932180	IMR90	lung:	n/a	chr3:47932017-47932028 chr3:47932018-47932027 chr3:47932016-47932027
44	CEBPB	chr3:48006277-48006512	Hela-S3	cervix:	n/a	chr3:48006478-48006489
45	CEBPB	chr3:48006243-48006691	HepG2	liver:	n/a	chr3:48006478-48006489
46	CEBPB	chr3:47979773-47980083	IMR90	lung:	n/a	chr3:47979919-47979930
47	CEBPB	chr3:47979857-47980059	Hela-S3	cervix:	n/a	chr3:47979919-47979930
48	CEBPB	chr3:48006086-48006567	K562	blood:	n/a	chr3:48006182-48006195 chr3:48006478-48006489
49	CEBPB	chr3:47942840-47943105	IMR90	lung:	n/a	chr3:47942971-47942982
50	CEBPB	chr3:48006139-48006654	HepG2	liver:	n/a	chr3:48006182-48006195 chr3:48006478-48006489

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47932918-47932968	Hela-S3	cervix:	n/a
2	chr3:48004832-48004882	HL-60	blood:	n/a
3	chr3:47952098-47952148	CMK	blood:	n/a
4	chr3:47933600-47933650	HEK293	kidney:	embryo
5	chr3:48004832-48004882	GM12878	blood:	n/a
6	chr3:48004832-48004882	GM06990	blood:	n/a
7	chr3:47952841-47952891	SAEC	small airway:	n/a
8	chr3:47933600-47933650	Hela-S3	cervix:	n/a
9	chr3:47952509-47952559	T-47D	breast:	n/a
10	chr3:47952509-47952559	SK-N-MC	brain:	n/a
11	chr3:47933600-47933650	HCPEpiC	choroid plexus:	n/a
12	chr3:47932918-47932968	HUVEC	blood vessel:	n/a
13	chr3:47952509-47952559	ECC-1	luminal epithelium:	n/a
14	chr3:47932918-47932968	HIPEpiC	eye:	n/a
15	chr3:47932918-47932968	HRE	kidney:	n/a
16	chr3:48004832-48004882	HRCEpiC	kidney:	n/a
17	chr3:48004832-48004882	ECC-1	luminal epithelium:	n/a
18	chr3:47952841-47952891	GM06990	blood:	n/a
19	chr3:47950807-47950857	MCF-7	breast:	n/a
20	chr3:47952509-47952559	LNCaP	prostate:	n/a
21	chr3:47950807-47950857	BJ	skin:	n/a
22	chr3:47933600-47933650	MCF10A-Er-Src	breast:	n/a
23	chr3:47952841-47952891	HRE	kidney:	n/a
24	chr3:47952509-47952559	PrEC	prostate:	n/a
25	chr3:47952098-47952148	AG04449	skin:	fetal
26	chr3:47933600-47933650	BE2_C	brain:	n/a
27	chr3:47952098-47952148	A549	lung:	n/a
28	chr3:47932918-47932968	ECC-1	luminal epithelium:	n/a
29	chr3:47952509-47952559	HL-60	blood:	n/a
30	chr3:47932918-47932968	MCF-7	breast:	n/a
31	chr3:47952509-47952559	GM12891	blood:	n/a
32	chr3:48004832-48004882	SK-N-SH_RA	brain:	n/a
33	chr3:47932918-47932968	SKMC	muscle:	n/a
34	chr3:47950807-47950857	A549	lung:	n/a
35	chr3:47952098-47952148	Jurkat	blood:	n/a
36	chr3:47950807-47950857	ovcar-3	ovarian:	n/a
37	chr3:47952509-47952559	HNPCEpiC	eye:	n/a
38	chr3:47952509-47952559	SK-N-SH	brain:	n/a
39	chr3:47952098-47952148	HEK293	kidney:	embryo
40	chr3:47952611-47952661	GM12892	blood:	n/a
41	chr3:47950807-47950857	Jurkat	blood:	n/a
42	chr3:47952098-47952148	AG09319	gingival:	n/a
43	chr3:47932918-47932968	ovcar-3	ovarian:	n/a
44	chr3:47933600-47933650	HPAEpiC	pulmonary alveolar:	n/a
45	chr3:47932918-47932968	NHDF-neo	bronchial:	n/a
46	chr3:47952611-47952661	HAEpiC	amniotic membrane:	n/a
47	chr3:47950807-47950857	IMR90	lung:	fetal
48	chr3:47932918-47932968	GM12892	blood:	n/a
49	chr3:47932918-47932968	BJ	skin:	n/a
50	chr3:47952841-47952891	ovcar-3	ovarian:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:47915163..47917361-chr3:47919966..47922770,2	K562	blood:
2	chr3:47976597..47979542-chr3:47982798..47984829,3	K562	blood:
3	chr3:47954841..47956498-chr3:47961686..47964207,2	K562	blood:
4	chr3:47952765..47954649-chr3:47957193..47959819,2	K562	blood:
5	chr3:47988815..47991729-chr3:47994715..47997497,2	K562	blood:
6	chr3:47912898..47916471-chr3:47916920..47919388,4	K562	blood:
7	chr3:47940568..47943002-chr3:47944240..47946560,3	K562	blood:
8	chr3:47976597..47979542-chr3:47982798..47984829,3	K562	blood:
9	chr3:47843314..47845660-chr3:47950504..47953455,2	MCF-7	breast:
10	chr3:47931648..47933684-chr3:47942643..47945311,2	K562	blood:
11	chr3:47928304..47929977-chr3:47930679..47933276,2	K562	blood:
12	chr3:47988815..47991729-chr3:47994715..47997497,2	K562	blood:
13	chr3:47940250..47943002-chr3:47945060..47946714,2	K562	blood:
14	chr3:47988815..47992482-chr3:47994715..47997497,3	K562	blood:
15	chr3:47908132..47910392-chr3:47951934..47954399,2	K562	blood:
16	chr3:47930805..47933794-chr3:47935046..47936999,2	K562	blood:
17	chr3:47940568..47943002-chr3:47944240..47946560,3	K562	blood:
18	chr3:47961751..47964593-chr3:47965535..47967248,2	K562	blood:
19	chr3:47866518..47868844-chr3:47913632..47916237,2	K562	blood:
20	chr3:47959598..47961533-chr3:47965469..47967262,2	K562	blood:
21	chr3:47952012..47952532-chr3:111085239..111085759,2	MCF-7	breast:
22	chr3:47908495..47911109-chr3:47911186..47914669,4	K562	blood:
23	chr3:47941256..47942794-chr3:47951029..47952546,2	MCF-7	breast:
24	chr3:47954841..47956498-chr3:47961686..47964207,2	K562	blood:
25	chr3:47965405..47966999-chr3:47969364..47970935,2	K562	blood:
26	chr3:47919145..47920888-chr3:47933987..47935579,2	K562	blood:
27	chr3:47995817..47998198-chr3:48000439..48002140,2	K562	blood:
28	chr3:47988815..47992482-chr3:47994715..47997497,3	K562	blood:
29	chr3:47952765..47954649-chr3:47957193..47959819,2	K562	blood:
30	chr3:47917882..47919572-chr3:47936119..47938317,2	K562	blood:
31	chr3:47919145..47920888-chr3:47933987..47935579,2	K562	blood:
32	chr3:47961751..47964593-chr3:47965535..47967248,2	K562	blood:
33	chr3:47865438..47868063-chr3:47949472..47951050,2	K562	blood:
34	chr3:47948658..47950260-chr3:47950870..47952844,2	K562	blood:
35	chr3:47947689..47949234-chr3:47950366..47953123,2	K562	blood:
36	chr3:47995817..47998198-chr3:48000439..48002140,2	K562	blood:
37	chr3:47970944..47972483-chr3:47977512..47980509,2	K562	blood:
38	chr3:47915163..47917361-chr3:47919966..47922770,2	K562	blood:
39	chr3:47977230..47979542-chr3:47982942..47984829,2	K562	blood:
40	chr3:47970944..47972483-chr3:47977512..47980509,2	K562	blood:
41	chr3:47935127..47936630-chr3:47951043..47952545,2	K562	blood:
42	chr3:47898431..47902857-chr3:47908612..47913870,6	K562	blood:
43	chr3:47940250..47943002-chr3:47945060..47946714,2	K562	blood:
44	chr3:47977230..47979542-chr3:47982942..47984829,2	K562	blood:
45	chr3:47959598..47961533-chr3:47965469..47967262,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMARCC1-4	chr3:48001817-48002571	NONHSAT089536
2	lnc-SMARCC1-3	chr3:47912738-47912776	NONHSAT089533
3	lnc-SMARCC1-3	chr3:47913407-47913590	NONHSAT089533
4	lnc-SMARCC1-3	chr3:47918907-47919255	NONHSAT089533

No data

Variant related genes	Relation type
MAP4	TF binding region
VPS26BP1	TF binding region
ENSG00000199591	TF binding region
MAP4	CpG island
VPS26BP1	CpG island
ENSG00000199591	CpG island
ENSG00000047849	chromatin interactions
ENSG00000132153	chromatin interactions

Extended variants
information (count: 3365 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3365 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17729010	chr3:47912703-47912704	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376827214	chr3:47912717-47912718	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs367816245	chr3:47912723-47912724	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144537836	chr3:47912736-47912737	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs139473425	chr3:47912742-47912743	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs542341878	chr3:47912755-47912756	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs183527842	chr3:47912782-47912783	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs531285532	chr3:47912783-47912784	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550504636	chr3:47912840-47912841	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565616331	chr3:47912975-47912976	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532849885	chr3:47912994-47912995	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547995019	chr3:47913009-47913010	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555940474	chr3:47913022-47913023	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574261423	chr3:47913045-47913046	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs144860225	chr3:47913065-47913066	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs111793212	chr3:47913083-47913084	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374111822	chr3:47913259-47913260	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530224428	chr3:47913289-47913290	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188691685	chr3:47913295-47913296	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569720152	chr3:47913306-47913307	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537009677	chr3:47913347-47913348	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147921210	chr3:47913351-47913352	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377238920	chr3:47913384-47913385	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530788545	chr3:47913404-47913405	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116732875	chr3:47913425-47913426	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs538536142	chr3:47913426-47913427	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs553967485	chr3:47913429-47913430	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs112516700	chr3:47913430-47913431	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs141377841	chr3:47913435-47913436	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs138793102	chr3:47913464-47913465	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs143669663	chr3:47913472-47913473	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs572112497	chr3:47913482-47913483	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs369799584	chr3:47913490-47913491	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs34711403	chr3:47913498-47913499	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs373873361	chr3:47913549-47913550	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs139797326	chr3:47913559-47913560	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs141252938	chr3:47913588-47913589	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs375636971	chr3:47913593-47913594	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs372960967	chr3:47913631-47913632	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554016844	chr3:47913672-47913673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543488752	chr3:47913683-47913684	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs564851119	chr3:47913684-47913685	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs532888905	chr3:47913696-47913697	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541325732	chr3:47913704-47913705	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs367692759	chr3:47913740-47913741	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559920778	chr3:47913759-47913760	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs559772222	chr3:47913995-47913996	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532077317	chr3:47914014-47914015	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371485097	chr3:47914021-47914022	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs199751749	chr3:47914052-47914053	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2784 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47867800-47918800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr3:47868000-47915200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:47868400-47916400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:47868400-47919000	Strong transcription	Fetal Stomach	stomach
5	chr3:47869000-47918600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr3:47870800-47931800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr3:47884600-47918400	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr3:47885000-47914800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:47894800-47917400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr3:47894800-47919400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:47896600-47919600	Strong transcription	Fetal Muscle Trunk	muscle
12	chr3:47896800-47913200	Strong transcription	Fetal Muscle Leg	muscle
13	chr3:47899000-47919000	Weak transcription	Right Atrium	heart
14	chr3:47903800-47915800	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr3:47904000-47915000	Strong transcription	Ovary	ovary
16	chr3:47904000-47915600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:47904000-47918600	Strong transcription	Osteobl	bone
18	chr3:47904200-47913600	Strong transcription	Brain Germinal Matrix	brain
19	chr3:47904200-47915400	Strong transcription	Stomach Smooth Muscle	stomach
20	chr3:47904200-47917400	Strong transcription	HSMM	muscle
21	chr3:47904200-47917400	Strong transcription	NH-A	brain
22	chr3:47904200-47917600	Strong transcription	Duodenum Smooth Muscle	Duodenum
23	chr3:47904200-47918600	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr3:47904400-47915200	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr3:47904400-47916400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr3:47904600-47912800	Strong transcription	Duodenum Mucosa	Duodenum
27	chr3:47904600-47915000	Strong transcription	Colon Smooth Muscle	Colon
28	chr3:47904600-47918600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr3:47904600-47918800	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr3:47904600-47919000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:47904800-47913000	Strong transcription	Gastric	stomach
32	chr3:47904800-47913600	Strong transcription	Brain Anterior Caudate	brain
33	chr3:47904800-47914800	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr3:47904800-47914800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:47904800-47914800	Strong transcription	HMEC	breast
36	chr3:47904800-47915000	Strong transcription	Fetal Brain Female	brain
37	chr3:47904800-47915000	Strong transcription	HepG2	liver
38	chr3:47904800-47915200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr3:47904800-47915200	Strong transcription	Fetal Thymus	thymus
40	chr3:47904800-47915400	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr3:47904800-47915400	Strong transcription	Primary T cells from cord blood	blood
42	chr3:47904800-47915400	Strong transcription	NHLF	lung
43	chr3:47904800-47916000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:47904800-47916400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr3:47904800-47916400	Strong transcription	NHEK	skin
46	chr3:47904800-47917400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:47904800-47917400	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr3:47904800-47917400	Strong transcription	Skeletal Muscle Male	skeletal muscle
49	chr3:47904800-47917400	Strong transcription	Dnd41	blood
50	chr3:47904800-47917400	Strong transcription	HSMMtube	muscle

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