Variant report

Variant	esv3375632
Chromosome Location	chr4:2941604-2944102
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:366)
Chromatin interactive
region (count:12)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:2941880-2942238	A549	lung:	n/a	n/a
2	BCL3	chr4:2942454-2942946	GM12878	blood:	n/a	n/a
3	BCL3	chr4:2943241-2943554	GM12878	blood:	n/a	n/a
4	BCL3	chr4:2942414-2943286	A549	lung:	n/a	n/a
5	CCNT2	chr4:2942888-2943333	K562	blood:	n/a	n/a
6	CHD2	chr4:2943340-2943758	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr4:2942090-2942163	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr4:2942571-2942957	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr4:2943842-2943932	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr4:2943636-2943659	MCF-7	breast:	n/a	n/a
11	CTCF	chr4:2943280-2943430	GM12864	blood:	n/a	n/a
12	CTCF	chr4:2943561-2943585	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr4:2943640-2943790	NHEK	skin:	n/a	n/a
14	CTCF	chr4:2943246-2943302	GM12891	blood:	n/a	n/a
15	CTCF	chr4:2943276-2943315	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:2943640-2943660	GM19238	blood:	n/a	n/a
17	ELF1	chr4:2943908-2944541	GM12878	blood:	n/a	n/a
18	ELF1	chr4:2942255-2942974	GM12878	blood:	n/a	n/a
19	GTF2F1	chr4:2941861-2941892	K562	blood:	n/a	n/a
20	JUND	chr4:2942569-2942878	A549	lung:	n/a	n/a
21	JUND	chr4:2943245-2943535	A549	lung:	n/a	n/a
22	JUND	chr4:2943915-2944199	A549	lung:	n/a	n/a
23	MTA3	chr4:2943619-2945276	GM12878	blood:	n/a	n/a
24	MTA3	chr4:2942195-2942986	GM12878	blood:	n/a	n/a
25	MYC	chr4:2942465-2942479	MCF-7	breast:	n/a	n/a
26	MYC	chr4:2942484-2942505	MCF-7	breast:	n/a	n/a
27	MYC	chr4:2942515-2942526	MCF-7	breast:	n/a	n/a
28	NFATC1	chr4:2943727-2944657	GM12878	blood:	n/a	n/a
29	NFATC1	chr4:2941624-2942392	GM12878	blood:	n/a	n/a
30	PML	chr4:2943087-2944262	GM12878	blood:	n/a	n/a
31	PML	chr4:2941728-2942859	GM12878	blood:	n/a	n/a
32	POLR2A	chr4:2941634-2941647	MCF-7	breast:	n/a	n/a
33	POLR2A	chr4:2941637-2942007	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr4:2941900-2945918	U87	brain:	n/a	n/a
35	POLR2A	chr4:2942930-2943546	GM12878	blood:	n/a	n/a
36	POLR2A	chr4:2941982-2942132	A549	lung:	n/a	n/a
37	POLR2A	chr4:2942168-2942381	HCT-116	colon:	n/a	n/a
38	POLR2A	chr4:2943761-2945107	NB4	blood:	n/a	n/a
39	POLR2A	chr4:2943815-2945121	A549	lung:	n/a	n/a
40	POLR2A	chr4:2940538-2945308	GM12891	blood:	n/a	n/a
41	POLR2A	chr4:2940457-2946099	A549	lung:	n/a	n/a
42	POLR2A	chr4:2943223-2945194	K562	blood:	n/a	n/a
43	POLR2A	chr4:2941748-2941850	A549	lung:	n/a	n/a
44	POLR2A	chr4:2942208-2943481	GM12891	blood:	n/a	n/a
45	POLR2A	chr4:2941392-2942941	HCT-116	colon:	n/a	n/a
46	POLR2A	chr4:2941719-2941850	A549	lung:	n/a	n/a
47	POLR2A	chr4:2940541-2945723	GM12892	blood:	n/a	n/a
48	POLR2A	chr4:2942153-2943641	PBDE	blood:	n/a	n/a
49	POLR2A	chr4:2942473-2942477	MCF-7	breast:	n/a	n/a
50	POLR2A	chr4:2940661-2944919	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2944050-2944100	PFSK-1	brain:	n/a
2	chr4:2944050-2944100	SK-N-SH_RA	brain:	n/a
3	chr4:2944050-2944100	AG04449	skin:	fetal
4	chr4:2941570-2941620	SK-N-SH	brain:	n/a
5	chr4:2944050-2944100	Caco-2	colon:	n/a
6	chr4:2941570-2941620	T-47D	breast:	n/a
7	chr4:2941570-2941620	U87	brain:	n/a
8	chr4:2942425-2942475	ovcar-3	ovarian:	n/a
9	chr4:2941760-2941810	PFSK-1	brain:	n/a
10	chr4:2943901-2943951	AG09309	skin:	n/a
11	chr4:2943901-2943951	PANC-1	pancreas:	n/a
12	chr4:2941760-2941810	HRCEpiC	kidney:	n/a
13	chr4:2942362-2942412	SK-N-SH	brain:	n/a
14	chr4:2944050-2944100	NB4	blood:	n/a
15	chr4:2941760-2941810	K562	blood:	n/a
16	chr4:2943901-2943951	HRE	kidney:	n/a
17	chr4:2942362-2942412	AG09319	gingival:	n/a
18	chr4:2941570-2941620	Hepatocyte	liver:	n/a
19	chr4:2943901-2943951	Hepatocyte	liver:	n/a
20	chr4:2944050-2944100	HCT-116	colon:	n/a
21	chr4:2942425-2942475	PANC-1	pancreas:	n/a
22	chr4:2941760-2941810	SAEC	small airway:	n/a
23	chr4:2942362-2942412	IMR90	lung:	fetal
24	chr4:2942425-2942475	AG04449	skin:	fetal
25	chr4:2941570-2941620	HEEpiC	esophagus:	n/a
26	chr4:2942425-2942475	AG04450	lung:	fetal
27	chr4:2942425-2942475	PrEC	prostate:	n/a
28	chr4:2944050-2944100	HL-60	blood:	n/a
29	chr4:2941570-2941620	HMEC	breast:	n/a
30	chr4:2942362-2942412	HPAEpiC	pulmonary alveolar:	n/a
31	chr4:2941760-2941810	NB4	blood:	n/a
32	chr4:2944050-2944100	A549	lung:	n/a
33	chr4:2941570-2941620	Jurkat	blood:	n/a
34	chr4:2941760-2941810	AG04450	lung:	fetal
35	chr4:2943901-2943951	BJ	skin:	n/a
36	chr4:2944050-2944100	Hepatocyte	liver:	n/a
37	chr4:2941570-2941620	SK-N-SH_RA	brain:	n/a
38	chr4:2941760-2941810	ECC-1	luminal epithelium:	n/a
39	chr4:2942425-2942475	HUVEC	blood vessel:	n/a
40	chr4:2941760-2941810	HCM	heart:	n/a
41	chr4:2941570-2941620	HCF	heart:	n/a
42	chr4:2941570-2941620	AG04449	skin:	fetal
43	chr4:2941570-2941620	BE2_C	brain:	n/a
44	chr4:2944050-2944100	U87	brain:	n/a
45	chr4:2943901-2943951	AG04450	lung:	fetal
46	chr4:2942425-2942475	LNCaP	prostate:	n/a
47	chr4:2942425-2942475	HRE	kidney:	n/a
48	chr4:2942362-2942412	BE2_C	brain:	n/a
49	chr4:2942362-2942412	CMK	blood:	n/a
50	chr4:2941570-2941620	NT2-D1	testis:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2943953..2946628-chr4:2962400..2965288,3	MCF-7	breast:
2	chr11:62609089..62610637-chr4:2941968..2944079,2	MCF-7	breast:
3	chr4:2906552..2911481-chr4:2934891..2942965,11	MCF-7	breast:
4	chr4:2940357..2942863-chr4:2954214..2956464,2	K562	blood:
5	chr3:22963977..22966878-chr4:2943742..2946615,2	MCF-7	breast:
6	chr4:2907975..2910281-chr4:2941881..2943677,2	MCF-7	breast:
7	chr4:2844829..2846512-chr4:2941018..2943974,2	K562	blood:
8	chr4:2914761..2916351-chr4:2943871..2946049,2	K562	blood:
9	chr4:2798770..2801758-chr4:2941180..2943976,2	K562	blood:
10	chr4:2941284..2943346-chr4:2963790..2966270,3	MCF-7	breast:
11	chr17:700252..700898-chr4:2940705..2941671,2	Hela-S3	cervix:
12	chr4:2790052..2809152-chr4:2930639..2948075,83	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADD1-1	chr4:2942029-2943596	ENSG00000249673
2	lnc-ADD1-1	chr4:2942029-2942168	ENSG00000249673
3	lnc-ADD1-1	chr4:2942029-2943778	ENSG00000249673.2

No data

Variant related genes	Relation type
NOP14	TF binding region
NOP14	CpG island
ENSG00000125388	chromatin interactions
ENSG00000087274	chromatin interactions
ENSG00000087266	chromatin interactions
ENSG00000087269	chromatin interactions
ENSG00000133316	chromatin interactions
SLC11A2	miRNA target sites
KAT2B	miRNA target sites

Extended variants
information (count: 174 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:174 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs137865788	chr4:2941612-2941613	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs368319039	chr4:2941625-2941626	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs541941212	chr4:2941632-2941633	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs561874905	chr4:2941639-2941640	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs527767491	chr4:2941645-2941646	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs547511630	chr4:2941652-2941653	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs570820215	chr4:2941666-2941667	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs539055440	chr4:2941676-2941677	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs560042212	chr4:2941713-2941714	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs72484523	chr4:2941721-2941722	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs35935100	chr4:2941723-2941724	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs372335117	chr4:2941756-2941757	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs533458874	chr4:2941765-2941766	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs550463965	chr4:2941767-2941768	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs375884294	chr4:2941782-2941783	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs570286278	chr4:2941793-2941794	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs536086481	chr4:2941794-2941795	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs542057272	chr4:2941796-2941797	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs568103635	chr4:2941804-2941805	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs533883625	chr4:2941826-2941827	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs553492285	chr4:2941852-2941853	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs576731697	chr4:2941902-2941903	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs545707096	chr4:2941942-2941943	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs556011748	chr4:2941982-2941983	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs2032463	chr4:2941988-2941989	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs541653921	chr4:2941990-2941991	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs113960909	chr4:2942010-2942011	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs527826805	chr4:2942011-2942012	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs187154721	chr4:2942013-2942014	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs564341115	chr4:2942059-2942060	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs1475974	chr4:2942073-2942074	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs3204775	chr4:2942077-2942078	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs550179459	chr4:2942081-2942082	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs192020478	chr4:2942092-2942093	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs147152463	chr4:2942094-2942095	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs549645905	chr4:2942104-2942105	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs150630858	chr4:2942129-2942130	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs566219466	chr4:2942187-2942188	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs1063744	chr4:2942209-2942210	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549633131	chr4:2942239-2942240	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs571287469	chr4:2942244-2942245	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
42	rs557782571	chr4:2942288-2942289	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
43	rs77859132	chr4:2942296-2942297	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs182955240	chr4:2942309-2942310	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
45	rs116562124	chr4:2942312-2942313	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
46	rs555723799	chr4:2942335-2942336	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
47	rs187416899	chr4:2942345-2942346	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
48	rs142131638	chr4:2942364-2942365	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
49	rs535356224	chr4:2942367-2942368	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
50	rs555272655	chr4:2942370-2942371	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	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
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2937800-2941800	Weak transcription	Small Intestine	intestine
2	chr4:2937800-2942400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr4:2937800-2945800	Weak transcription	Fetal Kidney	kidney
4	chr4:2938000-2945400	Genic enhancers	Primary T cells fromperipheralblood	blood
5	chr4:2938000-2960400	Weak transcription	Right Atrium	heart
6	chr4:2938200-2946800	Strong transcription	Thymus	Thymus
7	chr4:2938200-2948400	Strong transcription	Fetal Intestine Small	intestine
8	chr4:2938200-2962200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:2938400-2944400	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr4:2938400-2957600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr4:2938400-2959600	Strong transcription	Brain Anterior Caudate	brain
12	chr4:2938400-2962200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr4:2938600-2943800	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr4:2938600-2949600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:2938600-2960400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr4:2938600-2960400	Strong transcription	Brain Cingulate Gyrus	brain
17	chr4:2938600-2961000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:2938600-2961600	Strong transcription	Primary T cells from cord blood	blood
19	chr4:2938600-2961600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:2938800-2944000	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr4:2938800-2955600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:2938800-2956800	Strong transcription	Fetal Intestine Large	intestine
23	chr4:2938800-2959200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:2938800-2961000	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr4:2938800-2961000	Strong transcription	Primary hematopoietic stem cells	blood
26	chr4:2938800-2961000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr4:2939000-2943000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr4:2939000-2956800	Strong transcription	H9 Cell Line	embryonic stem cell
29	chr4:2939000-2956800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr4:2939000-2957400	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr4:2939000-2958400	Strong transcription	Brain Substantia Nigra	brain
32	chr4:2939000-2960200	Strong transcription	Lung	lung
33	chr4:2939000-2961600	Strong transcription	Fetal Stomach	stomach
34	chr4:2939200-2953800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:2939200-2956200	Strong transcription	Left Ventricle	heart
36	chr4:2939200-2959200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:2939200-2959600	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr4:2939200-2960000	Strong transcription	Stomach Smooth Muscle	stomach
39	chr4:2939200-2960600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr4:2939200-2961000	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr4:2939200-2963200	Weak transcription	Fetal Heart	heart
42	chr4:2939400-2942600	Strong transcription	Esophagus	oesophagus
43	chr4:2939400-2944200	Strong transcription	Duodenum Mucosa	Duodenum
44	chr4:2939400-2945800	Strong transcription	HSMMtube	muscle
45	chr4:2939400-2948000	Strong transcription	Liver	Liver
46	chr4:2939400-2952600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:2939400-2956800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:2939400-2957200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:2939400-2959000	Strong transcription	Ovary	ovary
50	chr4:2939400-2959400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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