Variant report

Variant	esv1812438
Chromosome Location	chr4:68943858-69154222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1098)
CpG islands
(count:1163)
Chromatin interactive
region (count:41)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69133011-69133899	K562	blood:	n/a	n/a
2	ARID3A	chr4:69042402-69042475	K562	blood:	n/a	n/a
3	ARID3A	chr4:68995505-68995878	K562	blood:	n/a	n/a
4	ARID3A	chr4:69130002-69130028	K562	blood:	n/a	n/a
5	ATF1	chr4:69121959-69122424	K562	blood:	n/a	n/a
6	ATF1	chr4:69014644-69014829	K562	blood:	n/a	n/a
7	ATF1	chr4:69133136-69133799	K562	blood:	n/a	n/a
8	ATF1	chr4:69131895-69132155	K562	blood:	n/a	n/a
9	ATF1	chr4:69130896-69131204	K562	blood:	n/a	n/a
10	ATF1	chr4:69018227-69018433	K562	blood:	n/a	n/a
11	ATF1	chr4:68995507-68995848	K562	blood:	n/a	n/a
12	ATF3	chr4:68995610-68995980	K562	blood:	n/a	n/a
13	BACH1	chr4:68990022-68990381	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:69100294-69100367	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:69106381-69106661	K562	blood:	n/a	n/a
16	BACH1	chr4:69137557-69138352	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr4:69115111-69115437	GM12878	blood:	n/a	chr4:69115296-69115307 chr4:69115376-69115384
18	BCL11A	chr4:69115147-69115501	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:69109982-69110192	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:69115198-69115451	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:68995560-68995938	K562	blood:	n/a	n/a
22	BHLHE40	chr4:69138568-69138734	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:69151973-69151987	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:69121233-69121402	K562	blood:	n/a	n/a
25	BRCA1	chr4:69046738-69047214	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr4:69041334-69041564	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr4:69041302-69041592	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr4:69037905-69038216	K562	blood:	n/a	n/a
29	CBX3	chr4:69129410-69129643	K562	blood:	n/a	n/a
30	CBX3	chr4:69147378-69147755	K562	blood:	n/a	n/a
31	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
32	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
33	CBX3	chr4:69012824-69013135	K562	blood:	n/a	n/a
34	CBX3	chr4:69129396-69129774	K562	blood:	n/a	n/a
35	CBX3	chr4:69133168-69133712	K562	blood:	n/a	n/a
36	CBX3	chr4:69012748-69013185	K562	blood:	n/a	n/a
37	CBX3	chr4:69074794-69075040	K562	blood:	n/a	n/a
38	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
39	CEBPB	chr4:69049105-69049380	A549	lung:	n/a	chr4:69049268-69049279
40	CEBPB	chr4:69151511-69151639	K562	blood:	n/a	n/a
41	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
42	CEBPB	chr4:69086517-69086666	K562	blood:	n/a	n/a
43	CEBPB	chr4:69046723-69047292	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:69134424-69134628	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:69041350-69041567	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:69015863-69016001	K562	blood:	n/a	chr4:69015942-69015953
47	CEBPB	chr4:69093019-69093284	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
49	CEBPB	chr4:69043232-69043529	IMR90	lung:	n/a	chr4:69043363-69043374
50	CEBPB	chr4:69095586-69095599	A549	lung:	n/a	n/a

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69048335-69048385	AG04449	skin:	fetal
2	chr4:69048156-69048206	SKMC	muscle:	n/a
3	chr4:69048335-69048385	T-47D	breast:	n/a
4	chr4:69048233-69048283	PANC-1	pancreas:	n/a
5	chr4:69048335-69048385	AG04449	skin:	fetal
6	chr4:69048156-69048206	SKMC	muscle:	n/a
7	chr4:69048335-69048385	T-47D	breast:	n/a
8	chr4:69048233-69048283	PANC-1	pancreas:	n/a
9	chr4:69048156-69048206	SAEC	small airway:	n/a
10	chr4:69046856-69046906	SK-N-SH	brain:	n/a
11	chr4:69052173-69052223	HRCEpiC	kidney:	n/a
12	chr4:69138730-69138780	HCT-116	colon:	n/a
13	chr4:69045141-69045191	BE2_C	brain:	n/a
14	chr4:69048335-69048385	NT2-D1	testis:	n/a
15	chr4:69052173-69052223	Caco-2	colon:	n/a
16	chr4:69084723-69084773	BE2_C	brain:	n/a
17	chr4:69048001-69048051	ProgFib	skin:	n/a
18	chr4:68995759-68995809	NT2-D1	testis:	n/a
19	chr4:69045141-69045191	RPTEC	kidney:	n/a
20	chr4:69047758-69047808	NHBE	bronchial:	n/a
21	chr4:69046856-69046906	NHDF-neo	bronchial:	n/a
22	chr4:69102304-69102354	HL-60	blood:	n/a
23	chr4:69048001-69048051	HCPEpiC	choroid plexus:	n/a
24	chr4:69048335-69048385	HRCEpiC	kidney:	n/a
25	chr4:69111580-69111630	A549	lung:	n/a
26	chr4:69083729-69083779	GM19239	blood:	n/a
27	chr4:69052173-69052223	AoSMC	blood vessel:	n/a
28	chr4:69102304-69102354	T-47D	breast:	n/a
29	chr4:69052173-69052223	SK-N-MC	brain:	n/a
30	chr4:69048001-69048051	SK-N-MC	brain:	n/a
31	chr4:69048335-69048385	HNPCEpiC	eye:	n/a
32	chr4:69111391-69111441	NHBE	bronchial:	n/a
33	chr4:69048335-69048385	AoSMC	blood vessel:	n/a
34	chr4:69054755-69054805	Jurkat	blood:	n/a
35	chr4:69054755-69054805	AG09309	skin:	n/a
36	chr4:69046856-69046906	ECC-1	luminal epithelium:	n/a
37	chr4:69054755-69054805	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:69084723-69084773	NT2-D1	testis:	n/a
39	chr4:69093675-69093725	HRPEpiC	eye:	n/a
40	chr4:69138730-69138780	HIPEpiC	eye:	n/a
41	chr4:69047758-69047808	AoSMC	blood vessel:	n/a
42	chr4:69093675-69093725	HepG2	liver:	n/a
43	chr4:68995759-68995809	Hepatocyte	liver:	n/a
44	chr4:69138730-69138780	RPTEC	kidney:	n/a
45	chr4:69054755-69054805	PFSK-1	brain:	n/a
46	chr4:69048001-69048051	ECC-1	luminal epithelium:	n/a
47	chr4:69045141-69045191	Hela-S3	cervix:	n/a
48	chr4:69093675-69093725	AG04449	skin:	fetal
49	chr4:69048430-69048480	HRE	kidney:	n/a
50	chr4:69054755-69054805	Hela-S3	cervix:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:68854785..68855326-chr4:69041026..69041997,2	MCF-7	breast:
2	chr1:180884197..180885718-chr4:69153705..69156603,2	MCF-7	breast:
3	chr4:69148927..69150978-chr4:69199918..69202560,2	K562	blood:
4	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
5	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
6	chr4:68853837..68854799-chr4:69040919..69041918,3	MCF-7	breast:
7	chr4:69143211..69145096-chr4:69239415..69241951,2	K562	blood:
8	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
9	chr4:68941725..68942553-chr4:69040855..69041893,4	MCF-7	breast:
10	chr4:68941684..68942576-chr4:69041048..69041788,2	K562	blood:
11	chr4:69104849..69107521-chr4:69108866..69110814,2	K562	blood:
12	chr4:69084812..69087062-chr4:69097475..69100132,2	K562	blood:
13	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
14	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
15	chr4:69152138..69154955-chr4:69200554..69203200,2	K562	blood:
16	chr4:69087616..69090439-chr4:69090621..69093039,2	K562	blood:
17	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
18	chr4:68945279..68946241-chr4:69040966..69041537,2	K562	blood:
19	chr4:69087616..69090439-chr4:69090621..69093039,2	K562	blood:
20	chr4:69137297..69138672-chr4:69241345..69242423,9	MCF-7	breast:
21	chr4:69078600..69080157-chr4:69085569..69088456,2	MCF-7	breast:
22	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
23	chr4:68945279..68946241-chr4:69040966..69041537,2	K562	blood:
24	chr4:69078600..69080157-chr4:69085569..69088456,2	MCF-7	breast:
25	chr4:69104849..69107521-chr4:69108866..69110814,2	K562	blood:
26	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
27	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
28	chr4:69050039..69052225-chr4:69055143..69056998,2	K562	blood:
29	chr4:69052749..69055570-chr4:69072267..69074922,2	MCF-7	breast:
30	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
31	chr4:68853962..68854562-chr4:69041076..69041834,2	K562	blood:
32	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
33	chr4:68784332..68784862-chr4:69040988..69041632,2	MCF-7	breast:
34	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
35	chr4:69084812..69087062-chr4:69097475..69100132,2	K562	blood:
36	chr4:68783821..68784619-chr4:69040970..69041992,6	MCF-7	breast:
37	chr4:68794157..68794866-chr4:69050816..69051359,2	MCF-7	breast:
38	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:
39	chr4:69052749..69055570-chr4:69072267..69074922,2	MCF-7	breast:
40	chr4:68784466..68787667-chr4:69042128..69044915,3	MCF-7	breast:
41	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS11BNL-1	chr4:69054121-69054474	NONHSAT096726
2	lnc-TMPRSS11BNL-1	chr4:69083624-69083721	NONHSAT096727
3	lnc-TMPRSS11E-1	chr4:68945839-68946670	ENSG00000248049
4	lnc-TMPRSS11BNL-1	chr4:69056739-69057034	NONHSAT096727
5	lnc-TMPRSS11E-1	chr4:68945839-68945944	ENSG00000248049
6	lnc-YTHDC1-2	chr4:69151533-69151677	NONHSAT096728
7	lnc-TMPRSS11BNL-1	chr4:69071753-69071815	NONHSAT096727
8	lnc-TMPRSS11E-5	chr4:69048010-69049221	NR_015446
9	lnc-YTHDC1-2	chr4:69149523-69149595	NONHSAT096728
10	lnc-TMPRSS11E-1	chr4:68945839-68946363	ENSG00000248049
11	lnc-TMPRSS11E-5	chr4:69051478-69051601	NR_015446
12	lnc-YTHDC1-2	chr4:69148179-69148398	NONHSAT096728
13	lnc-TMPRSS11E-5	chr4:69078024-69078188	NR_015446
14	lnc-TMPRSS11BNL-1	chr4:69078080-69078195	NONHSAT096727
15	lnc-TMPRSS11BNL-1	chr4:69071594-69071815	NONHSAT096726
16	lnc-TMPRSS11BNL-1	chr4:69083624-69083722	NONHSAT096726

No data

Variant related genes	Relation type
FTLP10	TF binding region
TMPRSS11B	TF binding region
TMPRSS11BNL	TF binding region
ENSG00000248639	TF binding region
TMPRSS11F	TF binding region
ENSG00000250642	TF binding region
ENSG00000250026	TF binding region
FTLP10	CpG island
TMPRSS11B	CpG island
TMPRSS11BNL	CpG island
ENSG00000248639	CpG island
TMPRSS11F	CpG island
ENSG00000250642	CpG island
ENSG00000250026	CpG island
ENSG00000270228	chromatin interactions
ENSG00000250026	chromatin interactions
ENSG00000162840	chromatin interactions
ENSG00000198092	chromatin interactions
ASPH	miRNA target sites
DICER1	miRNA target sites
RALGPS2	miRNA target sites

Extended variants
information (count: 4319 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4319 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371043346	chr4:68943864-68943865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200462885	chr4:68943973-68943974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575117415	chr4:68944030-68944031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573969206	chr4:68944050-68944051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191968950	chr4:68944052-68944053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144304968	chr4:68944101-68944102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148297594	chr4:68944115-68944116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530910423	chr4:68944173-68944174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs920297	chr4:68944214-68944215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs182116859	chr4:68944248-68944249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs920298	chr4:68944254-68944255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs546567979	chr4:68944265-68944266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566858219	chr4:68944269-68944270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529532995	chr4:68944274-68944275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549357567	chr4:68944319-68944320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569394545	chr4:68944337-68944338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186745323	chr4:68944352-68944353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77461651	chr4:68944369-68944370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571440634	chr4:68944391-68944392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373500524	chr4:68944453-68944454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551429657	chr4:68944610-68944611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77135316	chr4:68944615-68944616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530811558	chr4:68944656-68944657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10012085	chr4:68944667-68944668	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs550601997	chr4:68944679-68944680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553796987	chr4:68944728-68944729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574032920	chr4:68944739-68944740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75690859	chr4:68944743-68944744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143041948	chr4:68944744-68944745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182627770	chr4:68944747-68944748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78545920	chr4:68944749-68944750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376383026	chr4:68944769-68944770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564629895	chr4:68944776-68944777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536502472	chr4:68944791-68944792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6829596	chr4:68944795-68944796	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs188049141	chr4:68944826-68944827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147459034	chr4:68944830-68944831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553651824	chr4:68944859-68944860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529552974	chr4:68944867-68944868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12501540	chr4:68944869-68944870	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs562962562	chr4:68944947-68944948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140136998	chr4:68944979-68944980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553850142	chr4:68944996-68944997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551670338	chr4:68945043-68945044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571410641	chr4:68945066-68945067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533872000	chr4:68945085-68945086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547421131	chr4:68945101-68945102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567228816	chr4:68945107-68945108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539258301	chr4:68945150-68945151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368644858	chr4:68945156-68945157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Ollier disease	21235737	CNVD
Autism	21865298	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Thoracic aortic aneurysm	21698135	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Medulloblastoma	21163964	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68943800-68947800	Weak transcription	Esophagus	oesophagus
2	chr4:68945400-68946000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr4:68945400-68946200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr4:68945400-68946400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:68945400-68946400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:68945400-68946400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:68945600-68946000	Enhancers	H9 Cell Line	embryonic stem cell
8	chr4:68945600-68946000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:68945600-68946400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:68945600-68946400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:68945600-68946400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr4:68945600-68946400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:68947800-68949200	Enhancers	Esophagus	oesophagus
14	chr4:68964200-68964600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:68964400-68964800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr4:68964400-68965200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:68964600-68965000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:68964600-68965000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:68964600-68965200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:68964600-68965200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:68972000-68972400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr4:68979000-68979600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr4:68983400-68988000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:68987400-68989400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr4:68987400-68989400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr4:68987400-68989800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:68988000-68989600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr4:68988200-68989400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:68988600-68989600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:68989800-68995400	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr4:68991400-68991600	Enhancers	K562	blood
32	chr4:68991600-68991800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:68991600-68994600	Weak transcription	K562	blood
34	chr4:68993600-68993800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:68993600-68994000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:68994000-68994400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:68994400-68995000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:68994400-68995000	Enhancers	Placenta Amnion	Placenta Amnion
39	chr4:68994600-68995400	Enhancers	K562	blood
40	chr4:68995000-68995400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:68995000-68995400	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr4:68995200-68995400	Enhancers	NHEK	skin
43	chr4:68995400-68995600	Active TSS	Esophagus	oesophagus
44	chr4:68995400-68995800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:68995400-68995800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr4:68995400-68995800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:68995400-68996000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:68995400-68996000	Enhancers	H9 Cell Line	embryonic stem cell
49	chr4:68995400-68996000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:68995400-68996000	Enhancers	HMEC	breast

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