Variant report

Variant	esv1817375
Chromosome Location	chr4:8722240-9391741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4317)
CpG islands
(count:794)
Chromatin interactive
region (count:93)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4317 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9155684-9155703	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:9154835-9154872	HepG2	liver:	n/a	n/a
3	ATF1	chr4:9154438-9155046	K562	blood:	n/a	n/a
4	ATF3	chr4:9154337-9154466	K562	blood:	n/a	n/a
5	ATF3	chr4:8854995-8855309	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr4:8854977-8855363	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr4:8855081-8855244	K562	blood:	n/a	n/a
8	BACH1	chr4:8875855-8875971	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:8862941-8863709	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:8857632-8857756	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:8862268-8862627	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:8894725-8895016	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:8857031-8857091	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:8869917-8869990	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:8858777-8858889	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:8861399-8861529	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:8893693-8893726	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:8859610-8859971	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:8874989-8875170	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:8873787-8873987	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr4:9160170-9160447	GM12878	blood:	n/a	n/a
22	BATF	chr4:8947322-8947571	GM12878	blood:	n/a	chr4:8947446-8947457
23	BATF	chr4:9155872-9156200	GM12878	blood:	n/a	n/a
24	BATF	chr4:8877064-8877233	GM12878	blood:	n/a	chr4:8877125-8877134
25	BATF	chr4:8911262-8911579	GM12878	blood:	n/a	n/a
26	BATF	chr4:9075036-9075407	GM12878	blood:	n/a	n/a
27	BATF	chr4:9078532-9078952	GM12878	blood:	n/a	n/a
28	BATF	chr4:9027580-9027939	GM12878	blood:	n/a	n/a
29	BATF	chr4:8977979-8978183	GM12878	blood:	n/a	n/a
30	BATF	chr4:8947373-8947544	GM12878	blood:	n/a	chr4:8947446-8947457
31	BATF	chr4:8962972-8963416	GM12878	blood:	n/a	n/a
32	BATF	chr4:9074518-9074764	GM12878	blood:	n/a	n/a
33	BATF	chr4:9027584-9027898	GM12878	blood:	n/a	n/a
34	BATF	chr4:9125270-9125602	GM12878	blood:	n/a	n/a
35	BATF	chr4:9167731-9168069	GM12878	blood:	n/a	n/a
36	BATF	chr4:9069049-9069339	GM12878	blood:	n/a	n/a
37	BATF	chr4:9155377-9155748	GM12878	blood:	n/a	n/a
38	BATF	chr4:9383032-9383262	GM12878	blood:	n/a	n/a
39	BATF	chr4:9382976-9383219	GM12878	blood:	n/a	n/a
40	BATF	chr4:9050779-9051110	GM12878	blood:	n/a	n/a
41	BATF	chr4:9155849-9156145	GM12878	blood:	n/a	n/a
42	BATF	chr4:9075010-9075406	GM12878	blood:	n/a	n/a
43	BATF	chr4:9016052-9016284	GM12878	blood:	n/a	chr4:9016178-9016189
44	BATF	chr4:9059496-9059973	GM12878	blood:	n/a	n/a
45	BATF	chr4:9172276-9172654	GM12878	blood:	n/a	n/a
46	BATF	chr4:9019180-9019377	GM12878	blood:	n/a	n/a
47	BATF	chr4:9172306-9172654	GM12878	blood:	n/a	n/a
48	BATF	chr4:9078511-9078942	GM12878	blood:	n/a	n/a
49	BATF	chr4:9050852-9051138	GM12878	blood:	n/a	n/a
50	BATF	chr4:9170428-9170639	GM12878	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9382961-9383011	HEK293	kidney:	embryo
2	chr4:9382961-9383011	HEK293	kidney:	embryo
3	chr4:9355351-9355401	NB4	blood:	n/a
4	chr4:9352827-9352877	HCPEpiC	choroid plexus:	n/a
5	chr4:9382765-9382815	SAEC	small airway:	n/a
6	chr4:9385754-9385804	BE2_C	brain:	n/a
7	chr4:9382961-9383011	GM12891	blood:	n/a
8	chr4:9352827-9352877	HepG2	liver:	n/a
9	chr4:9355372-9355422	ProgFib	skin:	n/a
10	chr4:9385754-9385804	U87	brain:	n/a
11	chr4:9385754-9385804	CMK	blood:	n/a
12	chr4:9382066-9382116	AG04450	lung:	fetal
13	chr4:9382765-9382815	IMR90	lung:	fetal
14	chr4:8727474-8727524	Hela-S3	cervix:	n/a
15	chr4:9355372-9355422	HCT-116	colon:	n/a
16	chr4:9382066-9382116	HCT-116	colon:	n/a
17	chr4:9371043-9371093	HNPCEpiC	eye:	n/a
18	chr4:9382066-9382116	MCF10A-Er-Src	breast:	n/a
19	chr4:9355351-9355401	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:9371392-9371442	SK-N-SH_RA	brain:	n/a
21	chr4:9382961-9383011	Caco-2	colon:	n/a
22	chr4:9382953-9383003	PrEC	prostate:	n/a
23	chr4:9385754-9385804	NHDF-neo	bronchial:	n/a
24	chr4:9382961-9383011	SK-N-SH	brain:	n/a
25	chr4:9382765-9382815	T-47D	breast:	n/a
26	chr4:9352827-9352877	HEEpiC	esophagus:	n/a
27	chr4:9352827-9352877	Jurkat	blood:	n/a
28	chr4:9382953-9383003	HAEpiC	amniotic membrane:	n/a
29	chr4:9385754-9385804	AG10803	skin:	n/a
30	chr4:9382765-9382815	HRCEpiC	kidney:	n/a
31	chr4:9385754-9385804	H1-hESC	embryonic stem cell:	embryo
32	chr4:9379166-9379216	HIPEpiC	eye:	n/a
33	chr4:9382765-9382815	LNCaP	prostate:	n/a
34	chr4:9385754-9385804	HEK293	kidney:	embryo
35	chr4:9352827-9352877	HRPEpiC	eye:	n/a
36	chr4:9382961-9383011	U87	brain:	n/a
37	chr4:9355372-9355422	NHDF-neo	bronchial:	n/a
38	chr4:9355372-9355422	SK-N-MC	brain:	n/a
39	chr4:9355351-9355401	Caco-2	colon:	n/a
40	chr4:9382066-9382116	MCF-7	breast:	n/a
41	chr4:9352827-9352877	SK-N-SH	brain:	n/a
42	chr4:9382961-9383011	GM12878	blood:	n/a
43	chr4:9379166-9379216	PrEC	prostate:	n/a
44	chr4:9382066-9382116	HepG2	liver:	n/a
45	chr4:9355372-9355422	MCF-7	breast:	n/a
46	chr4:9382961-9383011	HIPEpiC	eye:	n/a
47	chr4:9383942-9383992	HCM	heart:	n/a
48	chr4:9383942-9383992	HUVEC	blood vessel:	n/a
49	chr4:9355372-9355422	U87	brain:	n/a
50	chr4:9383942-9383992	BE2_C	brain:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:8816885..8819513-chr4:8838676..8840311,2	K562	blood:
2	chr4:8689272..8690551-chr4:8887541..8888216,4	MCF-7	breast:
3	chr4:8667609..8668516-chr4:8887656..8888210,2	MCF-7	breast:
4	chr4:8987440..8989215-chr4:9123032..9125625,2	MCF-7	breast:
5	chr4:8722609..8725304-chr4:8746886..8749545,2	MCF-7	breast:
6	chr4:8609002..8610016-chr4:8919155..8920078,6	MCF-7	breast:
7	chr4:8987440..8989215-chr4:9123032..9125625,2	MCF-7	breast:
8	chr4:8743350..8745103-chr4:8747922..8749875,2	MCF-7	breast:
9	chr4:8840268..8842596-chr4:8847457..8849928,2	MCF-7	breast:
10	chr4:8648999..8649710-chr4:8883912..8884471,2	MCF-7	breast:
11	chr4:8821716..8822276-chr4:8919332..8919908,2	MCF-7	breast:
12	chr4:8847923..8849486-chr4:8849539..8851969,2	K562	blood:
13	chr4:8776407..8778118-chr4:8779629..8781870,2	MCF-7	breast:
14	chr4:8887296..8888159-chr4:8919813..8920332,3	MCF-7	breast:
15	chr4:8889120..8890631-chr4:8897595..8899572,2	MCF-7	breast:
16	chr4:8889120..8890631-chr4:8897595..8899572,2	MCF-7	breast:
17	chr4:8743350..8745103-chr4:8747922..8749875,2	MCF-7	breast:
18	chr4:8821602..8822427-chr4:8833992..8834964,2	MCF-7	breast:
19	chr4:8827560..8829523-chr4:8830683..8833064,2	K562	blood:
20	chr3:23845597..23847789-chr4:8879627..8881777,2	MCF-7	breast:
21	chr4:8785973..8787809-chr4:8789851..8791798,2	MCF-7	breast:
22	chr4:8917493..8920418-chr4:8922098..8924605,3	K562	blood:
23	chr4:8689647..8690533-chr4:8887295..8888077,4	K562	blood:
24	chr4:9155081..9155863-chr4:79696788..79697581,2	HCT-116	colon:
25	chr4:8827560..8829523-chr4:8830683..8833064,2	K562	blood:
26	chr4:8816885..8819513-chr4:8838676..8840311,2	K562	blood:
27	chr4:8874973..8877231-chr4:8879936..8882236,2	K562	blood:
28	chr4:8690025..8690993-chr4:8919534..8920174,2	MCF-7	breast:
29	chr4:8781022..8782784-chr4:8786066..8789038,2	K562	blood:
30	chr4:8781022..8782784-chr4:8786066..8789038,2	K562	blood:
31	chr4:8916094..8919081-chr4:8922098..8925711,3	K562	blood:
32	chr4:8821372..8822221-chr4:8847653..8848611,2	MCF-7	breast:
33	chr4:8840585..8842357-chr4:8849488..8852071,2	MCF-7	breast:
34	chr4:8847923..8849486-chr4:8849539..8851969,2	K562	blood:
35	chr4:8709792..8713378-chr4:8726638..8730577,3	K562	blood:
36	chr4:8701567..8704524-chr4:8729204..8732158,2	K562	blood:
37	chr4:8917493..8920418-chr4:8922098..8924605,3	K562	blood:
38	chr4:8778847..8780683-chr4:8898052..8900103,2	MCF-7	breast:
39	chr4:8747645..8749434-chr4:8754889..8757407,2	MCF-7	breast:
40	chr4:8677416..8680217-chr4:8770931..8773550,2	K562	blood:
41	chr4:8595963..8596810-chr4:8919438..8920172,2	MCF-7	breast:
42	chr4:8853371..8854874-chr4:8860134..8861698,2	K562	blood:
43	chr4:8821372..8822221-chr4:8847653..8848611,2	MCF-7	breast:
44	chr4:8738768..8740939-chr4:8744102..8745703,2	MCF-7	breast:
45	chr4:8840268..8842596-chr4:8847457..8849928,2	MCF-7	breast:
46	chr4:8649551..8650162-chr4:8919707..8920368,2	MCF-7	breast:
47	chr4:8609226..8610032-chr4:8887698..8888205,2	MCF-7	breast:
48	chr4:8894855..8897793-chr4:8901951..8903870,2	K562	blood:
49	chr4:8723681..8726595-chr4:8727045..8729022,2	MCF-7	breast:
50	chr4:8483492..8484345-chr4:8919742..8920371,2	MCF-7	breast:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMX1-4	chr4:9065968-9066056	NONHSAT095124
2	lnc-HMX1-4	chr4:9036310-9037271	NONHSAT095124
3	lnc-RP11-1396O13.13.1-2	chr4:9390589-9390785	l_2601_chr4:9381878-9390785_kidney
4	lnc-HMX1-1	chr4:8747123-8747482	ENSG00000250915
5	lnc-RP11-1396O13.13.1-1	chr4:9388003-9388085	XLOC_003878
6	lnc-RP11-1396O13.13.1-2	chr4:9381879-9382091	l_2601_chr4:9381878-9390785_kidney
7	lnc-HMX1-3	chr4:9053568-9053777	NONHSAT095125
8	lnc-HMX1-1	chr4:8747165-8747482	NONHSAT095114
9	lnc-HMX1-4	chr4:9072963-9073140	NONHSAT095124
10	lnc-HMX1-4	chr4:9065968-9066056	NONHSAT095122
11	lnc-HMX1-1	chr4:8749072-8749394	NONHSAT095113
12	lnc-ACOX3-3	chr4:8862375-8862553	ENSG00000258507.1
13	lnc-HMX1-1	chr4:8749072-8749394	NONHSAT095114
14	lnc-ACOX3-3	chr4:8860441-8860823	ENSG00000258507.1
15	lnc-RP11-1396O13.13.1-1	chr4:9376809-9376876	XLOC_003878
16	lnc-HMX1-4	chr4:9065968-9066056	NONHSAT095123
17	lnc-HMX1-4	chr4:9074628-9074691	NONHSAT095122
18	lnc-HMX1-4	chr4:9083355-9083373	NONHSAT095123
19	lnc-HMX1-1	chr4:8747656-8747863	NONHSAT095114
20	lnc-RP11-1396O13.13.1-1	chr4:9387384-9387466	XLOC_003878
21	lnc-RP11-1286E23.8.1-1	chr4:9174843-9174908	XLOC_003448
22	lnc-HMX1-4	chr4:9036251-9037271	NONHSAT095123
23	lnc-HMX1-4	chr4:9036251-9037271	NONHSAT095122
24	lnc-HMX1-1	chr4:8747672-8747863	NONHSAT095113
25	lnc-HMX1-1	chr4:8747656-8747759	ENSG00000250915
26	lnc-HMX1-2	chr4:9022583-9022887	NONHSAT095120
27	lnc-HMX1-1	chr4:8747165-8747482	NONHSAT095113
28	lnc-RP11-1286E23.8.1-1	chr4:9173538-9173895	XLOC_003448

No data

Variant related genes	Relation type
FAM86KP	TF binding region
ENSG00000258507	TF binding region
USP17L11	TF binding region
USP17L18	TF binding region
USP17L22	TF binding region
ENSG00000250342	TF binding region
ENSG00000271057	TF binding region
ENSG00000264372	TF binding region
ENSG00000251313	TF binding region
USP17L24	TF binding region
ENSG00000250804	TF binding region
USP17L29	TF binding region
USP17L13	TF binding region
HMX1	TF binding region
USP17L14P	TF binding region
ENSG00000197468	TF binding region
ENSG00000219492	TF binding region
USP17L12	TF binding region
ENSG00000238726	TF binding region
USP17L19	TF binding region
USP17L9P	TF binding region
USP17L5	TF binding region
ALG1L14P	TF binding region
USP17L10	TF binding region
UNC93B8	TF binding region
USP17L30	TF binding region
ENSG00000250915	TF binding region
FAM90A26	TF binding region
USP17L16P	TF binding region
USP17L17	TF binding region
ENPP7P10	TF binding region
USP17L21	TF binding region
USP17L15	TF binding region
USP17L26	TF binding region
USP17L23	TF binding region
ENSG00000249347	TF binding region
USP17L25	TF binding region
USP17L6P	TF binding region
USP17L27	TF binding region
USP17L20	TF binding region
USP17L28	TF binding region
FAM86KP	CpG island
ENSG00000258507	CpG island
USP17L11	CpG island
USP17L18	CpG island
USP17L22	CpG island
ENSG00000250342	CpG island
ENSG00000271057	CpG island
ENSG00000264372	CpG island
ENSG00000251313	CpG island
USP17L24	CpG island
ENSG00000250804	CpG island
USP17L29	CpG island
USP17L13	CpG island
HMX1	CpG island
USP17L14P	CpG island
ENSG00000197468	CpG island
ENSG00000219492	CpG island
USP17L12	CpG island
ENSG00000238726	CpG island
USP17L19	CpG island
USP17L9P	CpG island
USP17L5	CpG island
ALG1L14P	CpG island
USP17L10	CpG island
UNC93B8	CpG island
USP17L30	CpG island
ENSG00000250915	CpG island
FAM90A26	CpG island
USP17L16P	CpG island
USP17L17	CpG island
ENPP7P10	CpG island
USP17L21	CpG island
USP17L15	CpG island
USP17L26	CpG island
USP17L23	CpG island
ENSG00000249347	CpG island
USP17L25	CpG island
USP17L6P	CpG island
USP17L27	CpG island
USP17L20	CpG island
USP17L28	CpG island
ENSG00000087008	chromatin interactions
ENSG00000205959	chromatin interactions
ENSG00000260278	chromatin interactions
ENSG00000250915	chromatin interactions
ENSG00000258507	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000138756	chromatin interactions
ENSG00000170142	chromatin interactions
ENSG00000155275	chromatin interactions

Extended variants
information (count: 16902 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:16902 , 50 per page) page: 1 2 3 4 5 6 7 ... 339

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116328281	chr4:8722629-8722630	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs144522305	chr4:8722639-8722640	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552972610	chr4:8722652-8722653	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7679150	chr4:8722665-8722666	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs111478308	chr4:8722670-8722671	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535237916	chr4:8722696-8722697	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556760255	chr4:8722714-8722715	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs146624404	chr4:8722725-8722726	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545569770	chr4:8722726-8722727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs376863643	chr4:8722727-8722728	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557880437	chr4:8722732-8722733	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73090134	chr4:8722733-8722734	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs115191107	chr4:8722743-8722744	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs562331493	chr4:8722766-8722767	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544387312	chr4:8722792-8722793	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs182955398	chr4:8722799-8722800	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544768222	chr4:8722807-8722808	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs563085252	chr4:8722842-8722843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533617656	chr4:8722848-8722849	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562697654	chr4:8722851-8722852	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188754804	chr4:8722888-8722889	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs77136443	chr4:8722889-8722890	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111596975	chr4:8722890-8722891	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113944306	chr4:8722911-8722912	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs548981097	chr4:8722913-8722914	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs567986851	chr4:8722914-8722915	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536876148	chr4:8722984-8722985	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs4522850	chr4:8722990-8722991	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs143849019	chr4:8722998-8722999	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568706692	chr4:8723009-8723010	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs35646033	chr4:8723045-8723046	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs4507346	chr4:8723060-8723061	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs377520487	chr4:8723083-8723084	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7699356	chr4:8723092-8723093	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs193291298	chr4:8723118-8723119	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs78557112	chr4:8723177-8723178	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs555404175	chr4:8723193-8723194	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375046631	chr4:8723236-8723237	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544914781	chr4:8723245-8723246	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs73090136	chr4:8723257-8723258	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs578096186	chr4:8723294-8723295	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545620208	chr4:8723305-8723306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368684552	chr4:8723330-8723331	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527808553	chr4:8723346-8723347	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs111367172	chr4:8723350-8723351	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546679458	chr4:8723365-8723366	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560957747	chr4:8723385-8723386	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs148860021	chr4:8723423-8723424	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182734563	chr4:8723424-8723425	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs73090137	chr4:8723440-8723441	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Autism	21865298	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:2154 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8725400-8725600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr4:8725400-8726200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:8725600-8725800	Enhancers	H1 Cell Line	embryonic stem cell
4	chr4:8725800-8726600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr4:8726400-8726600	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
6	chr4:8726400-8726800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr4:8726400-8727000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:8726400-8727000	Enhancers	Pancreas	Pancrea
9	chr4:8726400-8727400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:8726400-8727400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:8726400-8728400	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr4:8726400-8728600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr4:8726600-8726800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr4:8726600-8726800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
15	chr4:8726600-8726800	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
16	chr4:8726600-8727000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr4:8726600-8727000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:8726600-8727000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:8726600-8727000	Enhancers	Gastric	stomach
20	chr4:8726600-8727200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:8726600-8728200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr4:8726800-8727000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:8726800-8727000	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
24	chr4:8726800-8727000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
25	chr4:8726800-8727200	Bivalent Enhancer	Stomach Mucosa	stomach
26	chr4:8727000-8727200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:8727000-8727600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
28	chr4:8727000-8728200	Bivalent Enhancer	Fetal Intestine Small	intestine
29	chr4:8727000-8729400	Weak transcription	Gastric	stomach
30	chr4:8727200-8728200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr4:8727400-8728600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:8727600-8727800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr4:8727600-8727800	Bivalent Enhancer	Fetal Intestine Large	intestine
34	chr4:8728200-8728400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:8728200-8728600	Enhancers	A549	lung
36	chr4:8728200-8732400	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr4:8728400-8730000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr4:8728600-8729000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:8729000-8730200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:8729200-8729400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:8729200-8729400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr4:8729200-8729800	Enhancers	Primary hematopoietic stem cells	blood
43	chr4:8729200-8729800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:8729400-8729800	Enhancers	Gastric	stomach
45	chr4:8729800-8731400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:8730000-8730200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr4:8730200-8730400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:8730400-8734000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:8734400-8734800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:8736800-8744800	Weak transcription	Right Atrium	heart

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