Variant report

Variant	nsv879701
Chromosome Location	chr4:107024776-107163128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:683)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:107122568-107122875	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:107158658-107158673	K562	blood:	n/a	n/a
3	ARID3A	chr4:107122500-107122908	K562	blood:	n/a	chr4:107122543-107122559 chr4:107122542-107122558
4	ATF2	chr4:107160021-107160295	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:107132367-107132419	K562	blood:	n/a	n/a
6	BCL3	chr4:107129042-107129310	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:107047305-107047313	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:107063996-107064001	GM12878	blood:	n/a	n/a
9	BRCA1	chr4:107159962-107160052	HepG2	liver:	n/a	n/a
10	CBX3	chr4:107083312-107083858	K562	blood:	n/a	n/a
11	CEBPB	chr4:107035494-107035721	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:107033292-107033530	HepG2	liver:	n/a	chr4:107033348-107033359
13	CEBPB	chr4:107033238-107033520	IMR90	lung:	n/a	chr4:107033348-107033359
14	CEBPB	chr4:107130226-107130488	Hela-S3	cervix:	n/a	chr4:107130336-107130349
15	CEBPB	chr4:107082153-107082403	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:107130258-107130471	K562	blood:	n/a	chr4:107130336-107130349
17	CEBPB	chr4:107113405-107113567	K562	blood:	n/a	n/a
18	CEBPB	chr4:107059048-107059329	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:107096804-107097116	IMR90	lung:	n/a	chr4:107096936-107096947
20	CEBPB	chr4:107130249-107130501	A549	lung:	n/a	chr4:107130336-107130349
21	CEBPB	chr4:107116003-107116285	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:107059051-107059306	A549	lung:	n/a	n/a
23	CEBPB	chr4:107123436-107123705	HepG2	liver:	n/a	chr4:107123585-107123596
24	CEBPB	chr4:107032062-107032136	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:107130215-107130494	IMR90	lung:	n/a	chr4:107130336-107130349
26	CEBPB	chr4:107123476-107123689	K562	blood:	n/a	chr4:107123585-107123596
27	CEBPB	chr4:107096846-107097088	HepG2	liver:	n/a	chr4:107096936-107096947
28	CEBPB	chr4:107068526-107068578	HepG2	liver:	n/a	chr4:107068539-107068550
29	CEBPB	chr4:107130236-107130498	HepG2	liver:	n/a	chr4:107130336-107130349
30	CEBPB	chr4:107083323-107083504	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:107033297-107033493	Hela-S3	cervix:	n/a	chr4:107033348-107033359
32	CTCF	chr4:107160100-107160250	GM12874	blood:	n/a	n/a
33	CTCF	chr4:107160160-107160310	GM12878	blood:	n/a	n/a
34	CTCF	chr4:107129860-107130010	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr4:107129683-107129869	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:107122640-107122790	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr4:107160100-107160250	GM12875	blood:	n/a	n/a
38	CTCF	chr4:107160100-107160250	GM12871	blood:	n/a	n/a
39	CTCF	chr4:107160076-107160310	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr4:107160140-107160290	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr4:107160065-107160255	GM19238	blood:	n/a	n/a
42	CTCF	chr4:107122694-107122798	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:107160108-107160273	GM10248	blood:	n/a	n/a
44	CTCF	chr4:107160160-107160310	K562	blood:	n/a	n/a
45	CTCF	chr4:107061880-107062030	HPAF	blood vessel:	n/a	chr4:107061936-107061954 chr4:107061931-107061952
46	CTCF	chr4:107122700-107122850	GM12872	blood:	n/a	n/a
47	CTCF	chr4:107122425-107123000	HCT-116	colon:	n/a	n/a
48	CTCF	chr4:107122540-107122690	GM12872	blood:	n/a	n/a
49	CTCF	chr4:107122620-107122770	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:107160120-107160270	HCM	heart:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:107130107-107130157	SK-N-SH	brain:	n/a
2	chr4:107130107-107130157	AG09319	gingival:	n/a
3	chr4:107130107-107130157	Hela-S3	cervix:	n/a
4	chr4:107130107-107130157	AoSMC	blood vessel:	n/a
5	chr4:107130107-107130157	HMEC	breast:	n/a
6	chr4:107130107-107130157	U87	brain:	n/a
7	chr4:107130107-107130157	HRCEpiC	kidney:	n/a
8	chr4:107130107-107130157	IMR90	lung:	fetal
9	chr4:107130107-107130157	CMK	blood:	n/a
10	chr4:107130107-107130157	HEK293	kidney:	embryo
11	chr4:107130107-107130157	HCM	heart:	n/a
12	chr4:107130107-107130157	GM06990	blood:	n/a
13	chr4:107130107-107130157	ProgFib	skin:	n/a
14	chr4:107130107-107130157	RPTEC	kidney:	n/a
15	chr4:107130107-107130157	BJ	skin:	n/a
16	chr4:107130107-107130157	AG04450	lung:	fetal
17	chr4:107130107-107130157	LNCaP	prostate:	n/a
18	chr4:107130107-107130157	NB4	blood:	n/a
19	chr4:107130107-107130157	SK-N-SH_RA	brain:	n/a
20	chr4:107130107-107130157	PFSK-1	brain:	n/a
21	chr4:107130107-107130157	GM12892	blood:	n/a
22	chr4:107130107-107130157	PrEC	prostate:	n/a
23	chr4:107130107-107130157	GM19239	blood:	n/a
24	chr4:107130107-107130157	HAEpiC	amniotic membrane:	n/a
25	chr4:107130107-107130157	AG09309	skin:	n/a
26	chr4:107130107-107130157	T-47D	breast:	n/a
27	chr4:107130107-107130157	GM12878	blood:	n/a
28	chr4:107130107-107130157	HIPEpiC	eye:	n/a
29	chr4:107130107-107130157	NHDF-neo	bronchial:	n/a
30	chr4:107130107-107130157	NH-A	brain:	n/a
31	chr4:107130107-107130157	Jurkat	blood:	n/a
32	chr4:107130107-107130157	MCF10A-Er-Src	breast:	n/a
33	chr4:107130107-107130157	K562	blood:	n/a
34	chr4:107130107-107130157	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:107130107-107130157	Caco-2	colon:	n/a
36	chr4:107130107-107130157	ECC-1	luminal epithelium:	n/a
37	chr4:107130107-107130157	HL-60	blood:	n/a
38	chr4:107130107-107130157	PANC-1	pancreas:	n/a
39	chr4:107130107-107130157	HEEpiC	esophagus:	n/a
40	chr4:107130107-107130157	HCPEpiC	choroid plexus:	n/a
41	chr4:107130107-107130157	AG04449	skin:	fetal
42	chr4:107130107-107130157	BE2_C	brain:	n/a
43	chr4:107130107-107130157	A549	lung:	n/a
44	chr4:107130107-107130157	HUVEC	blood vessel:	n/a
45	chr4:107130107-107130157	SK-N-MC	brain:	n/a
46	chr4:107130107-107130157	HRPEpiC	eye:	n/a
47	chr4:107130107-107130157	AG10803	skin:	n/a
48	chr4:107130107-107130157	NHBE	bronchial:	n/a
49	chr4:107130107-107130157	HNPCEpiC	eye:	n/a
50	chr4:107130107-107130157	H1-hESC	embryonic stem cell:	embryo

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:107057719..107060245-chr4:107065228..107066927,2	K562	blood:
2	chr4:107037209..107040065-chr4:107046985..107049286,2	K562	blood:
3	chr4:107116810..107118888-chr4:107121036..107122571,2	K562	blood:
4	chr4:106817148..106819269-chr4:107039233..107040831,3	MCF-7	breast:
5	chr4:107116810..107118888-chr4:107121036..107122571,2	K562	blood:
6	chr4:107144706..107146969-chr4:107150712..107153683,3	K562	blood:
7	chr4:106875594..106876144-chr4:107122239..107122877,2	MCF-7	breast:
8	chr4:107023929..107026888-chr4:107039825..107042203,2	K562	blood:
9	chr4:107160677..107162898-chr4:107235492..107237232,2	MCF-7	breast:
10	chr4:107129508..107131492-chr4:107132634..107135593,2	MCF-7	breast:
11	chr4:107142111..107144318-chr4:107145536..107147639,2	K562	blood:
12	chr4:107037209..107040065-chr4:107046985..107049286,2	K562	blood:
13	chr4:107057719..107060245-chr4:107065228..107066927,2	K562	blood:
14	chr4:107157087..107158697-chr4:107236510..107238674,2	MCF-7	breast:
15	chr4:106629937..106631659-chr4:107051139..107052653,2	MCF-7	breast:
16	chr4:107142111..107144318-chr4:107145536..107147639,2	K562	blood:
17	chr4:107023929..107026888-chr4:107039825..107042203,2	K562	blood:
18	chr4:106817910..106819582-chr4:107062720..107065633,2	MCF-7	breast:
19	chr4:107129974..107132069-chr4:107132979..107135565,2	MCF-7	breast:
20	chr2:88990302..88991116-chr4:107159175..107159797,2	MCF-7	breast:

No data

Variant related genes	Relation type
TBCK	TF binding region
TBCK	CpG island
ENSG00000138785	chromatin interactions
ENSG00000164022	chromatin interactions
ENSG00000145348	chromatin interactions
ENSG00000168743	chromatin interactions
ENSG00000138780	chromatin interactions

Extended variants
information (count: 4738 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4738 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10018910	chr4:107024776-107024777	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs193053142	chr4:107024824-107024825	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs573279929	chr4:107024857-107024858	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs545353106	chr4:107024871-107024872	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs565119143	chr4:107024876-107024877	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs530956684	chr4:107024933-107024934	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs184884918	chr4:107025020-107025021	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs35020147	chr4:107025054-107025055	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs34596530	chr4:107025061-107025062	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs563615849	chr4:107025119-107025120	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs572284663	chr4:107025152-107025153	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs555620955	chr4:107025172-107025173	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs78051958	chr4:107025201-107025202	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548906688	chr4:107025203-107025204	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs72964404	chr4:107025205-107025206	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs75414477	chr4:107025209-107025210	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577570307	chr4:107025218-107025219	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371247775	chr4:107025220-107025221	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375675353	chr4:107025232-107025233	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571132247	chr4:107025238-107025239	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543502212	chr4:107025257-107025258	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536691922	chr4:107025356-107025357	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368388024	chr4:107025358-107025359	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188478041	chr4:107025374-107025375	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575425698	chr4:107025425-107025426	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563281003	chr4:107025450-107025451	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs28805707	chr4:107025497-107025498	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs28784652	chr4:107025576-107025577	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs367935661	chr4:107025640-107025641	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs573418325	chr4:107025641-107025642	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs545151449	chr4:107025721-107025722	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs200544124	chr4:107025747-107025748	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs180988767	chr4:107025763-107025764	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs111898307	chr4:107025776-107025777	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs139202264	chr4:107025806-107025807	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563526385	chr4:107025826-107025827	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367644036	chr4:107025834-107025835	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73836981	chr4:107025838-107025839	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542770967	chr4:107025852-107025853	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs72964407	chr4:107025957-107025958	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs528314668	chr4:107026011-107026012	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185057851	chr4:107026014-107026015	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138589394	chr4:107026092-107026093	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530381485	chr4:107026132-107026133	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550186259	chr4:107026160-107026161	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187955681	chr4:107026165-107026166	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374616921	chr4:107026173-107026174	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536530208	chr4:107026174-107026175	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141142644	chr4:107026175-107026176	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72964409	chr4:107026181-107026182	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

Disease	PMID	Source
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cognitive impairment	21505072	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2086 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106997200-107031000	Weak transcription	Psoas Muscle	Psoas
2	chr4:107010200-107025400	Weak transcription	Small Intestine	intestine
3	chr4:107012400-107026800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr4:107012600-107025000	Weak transcription	Brain Substantia Nigra	brain
5	chr4:107012600-107025200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:107012600-107026200	Weak transcription	Stomach Mucosa	stomach
7	chr4:107012600-107026600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr4:107012600-107026600	Weak transcription	GM12878-XiMat	blood
9	chr4:107012600-107026600	Weak transcription	HSMM	muscle
10	chr4:107012600-107026800	Weak transcription	Fetal Kidney	kidney
11	chr4:107012600-107029800	Weak transcription	Fetal Brain Male	brain
12	chr4:107012600-107029800	Weak transcription	Dnd41	blood
13	chr4:107012600-107031200	Weak transcription	Brain Angular Gyrus	brain
14	chr4:107012600-107033200	Weak transcription	Osteobl	bone
15	chr4:107012600-107033800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr4:107012600-107034400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:107012600-107038400	Weak transcription	NHDF-Ad	bronchial
18	chr4:107012800-107024800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:107012800-107024800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr4:107012800-107024800	Weak transcription	Brain Hippocampus Middle	brain
21	chr4:107012800-107024800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr4:107012800-107025400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr4:107012800-107025400	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr4:107012800-107026200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr4:107012800-107030600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr4:107012800-107031400	Weak transcription	HSMMtube	muscle
27	chr4:107012800-107033400	Weak transcription	Rectal Smooth Muscle	rectum
28	chr4:107013000-107031000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:107014000-107024800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr4:107014000-107029800	Weak transcription	Brain Germinal Matrix	brain
31	chr4:107014000-107031000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:107014000-107031000	Weak transcription	Fetal Thymus	thymus
33	chr4:107014000-107031200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr4:107014000-107034600	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr4:107014200-107024800	Weak transcription	Esophagus	oesophagus
36	chr4:107014200-107024800	Weak transcription	Fetal Intestine Large	intestine
37	chr4:107014200-107024800	Weak transcription	Placenta	Placenta
38	chr4:107014200-107024800	Weak transcription	Thymus	Thymus
39	chr4:107014200-107024800	Weak transcription	Spleen	Spleen
40	chr4:107014200-107025000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:107014200-107025000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr4:107014200-107025000	Weak transcription	Aorta	Aorta
43	chr4:107014200-107025000	Weak transcription	Lung	lung
44	chr4:107014200-107025200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr4:107014200-107026000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:107014200-107026000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr4:107014200-107026000	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr4:107014200-107026200	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr4:107014200-107026200	Weak transcription	Fetal Brain Female	brain
50	chr4:107014200-107029200	Weak transcription	Sigmoid Colon	Sigmoid Colon

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