Variant report

Variant	esv3322278
Chromosome Location	chr4:3233604-3236102
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:98)
CpG islands
(count:732)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:98 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:3235484-3235883	K562	blood:	n/a	n/a
2	CEBPB	chr4:3233782-3233805	HepG2	liver:	n/a	n/a
3	CTCF	chr4:3235680-3235830	HVMF	connective:	n/a	n/a
4	CTCF	chr4:3235680-3235830	HAc	cerebellar:	n/a	n/a
5	CTCF	chr4:3235600-3235750	HFF-Myc	foreskin:	n/a	n/a
6	CTCF	chr4:3235600-3235750	SAEC	small airway:	n/a	n/a
7	CTCF	chr4:3235680-3235830	RPTEC	kidney:	n/a	n/a
8	CTCF	chr4:3235660-3235810	NB4	blood:	n/a	n/a
9	CTCF	chr4:3235661-3235828	K562	blood:	n/a	n/a
10	CTCF	chr4:3235660-3235810	BE2_C	brain:	n/a	n/a
11	CTCF	chr4:3235700-3235850	AG04449	skin:	n/a	n/a
12	CTCF	chr4:3235900-3236050	AG04449	skin:	n/a	n/a
13	CTCF	chr4:3235660-3235810	HA-sp	spinal cord:	n/a	n/a
14	CTCF	chr4:3235880-3236030	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr4:3235740-3235890	HFF	foreskin:	n/a	n/a
16	CTCF	chr4:3235720-3235870	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr4:3235660-3235810	AG09319	gingival:	n/a	n/a
18	CTCF	chr4:3235680-3235830	HEK293	kidney:	n/a	n/a
19	CTCF	chr4:3235680-3235830	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr4:3235580-3235730	BJ	skin:	n/a	n/a
21	CTCF	chr4:3235680-3235830	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr4:3235595-3235902	K562	blood:	n/a	n/a
23	CTCF	chr4:3235633-3235908	IMR90	lung:	n/a	n/a
24	CTCF	chr4:3235590-3235844	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr4:3235580-3235730	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr4:3235720-3235870	AG10803	skin:	n/a	n/a
27	CTCF	chr4:3235620-3235770	HMEC	breast:	n/a	n/a
28	CTCF	chr4:3235620-3235770	AG04449	skin:	n/a	n/a
29	CTCF	chr4:3235640-3235790	HPF	lung:	n/a	n/a
30	CTCF	chr4:3235680-3235830	BE2_C	brain:	n/a	n/a
31	CTCF	chr4:3235660-3235810	HepG2	liver:	n/a	n/a
32	CTCF	chr4:3235640-3235790	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr4:3235600-3235750	K562	blood:	n/a	n/a
34	CTCF	chr4:3235660-3235810	AG04450	lung:	n/a	n/a
35	CTCF	chr4:3235720-3235870	BJ	skin:	n/a	n/a
36	CTCF	chr4:3235700-3235850	AG09309	skin:	n/a	n/a
37	CTCF	chr4:3235640-3235790	GM06990	blood:	n/a	n/a
38	CTCF	chr4:3235640-3235790	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr4:3235720-3235870	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr4:3235640-3235790	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr4:3235680-3235830	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr4:3235707-3235776	GM12878	blood:	n/a	n/a
43	FOS	chr4:3235600-3235774	MCF10A-Er-Src	breast:	n/a	chr4:3235685-3235693 chr4:3235685-3235693 chr4:3235686-3235693
44	FOS	chr4:3235583-3235783	MCF10A-Er-Src	breast:	n/a	chr4:3235685-3235693 chr4:3235685-3235693 chr4:3235686-3235693
45	HMGN3	chr4:3235384-3235560	K562	blood:	n/a	n/a
46	JUN	chr4:3235395-3236020	K562	blood:	n/a	chr4:3235685-3235693 chr4:3235685-3235693 chr4:3235686-3235693
47	JUND	chr4:3235517-3235871	K562	blood:	n/a	chr4:3235685-3235693 chr4:3235685-3235693 chr4:3235686-3235693
48	JUND	chr4:3235579-3235779	H1-hESC	embryonic stem cell:	n/a	chr4:3235685-3235693 chr4:3235685-3235693 chr4:3235686-3235693
49	MAX	chr4:3235681-3235881	K562	blood:	n/a	chr4:3235736-3235745
50	MAZ	chr4:3235575-3235933	K562	blood:	n/a	chr4:3235736-3235745

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3235000-3235050	Caco-2	colon:	n/a
2	chr4:3234519-3234569	GM06990	blood:	n/a
3	chr4:3234519-3234569	AG09309	skin:	n/a
4	chr4:3234462-3234512	HUVEC	blood vessel:	n/a
5	chr4:3234519-3234569	SK-N-SH_RA	brain:	n/a
6	chr4:3233774-3233824	ECC-1	luminal epithelium:	n/a
7	chr4:3235295-3235345	GM12891	blood:	n/a
8	chr4:3234462-3234512	RPTEC	kidney:	n/a
9	chr4:3234814-3234864	HAEpiC	amniotic membrane:	n/a
10	chr4:3233774-3233824	HL-60	blood:	n/a
11	chr4:3234519-3234569	GM19239	blood:	n/a
12	chr4:3235589-3235639	GM12892	blood:	n/a
13	chr4:3233774-3233824	RPTEC	kidney:	n/a
14	chr4:3234519-3234569	LNCaP	prostate:	n/a
15	chr4:3233774-3233824	ProgFib	skin:	n/a
16	chr4:3235589-3235639	NB4	blood:	n/a
17	chr4:3235319-3235369	Jurkat	blood:	n/a
18	chr4:3234462-3234512	HL-60	blood:	n/a
19	chr4:3233865-3233915	K562	blood:	n/a
20	chr4:3234417-3234467	GM06990	blood:	n/a
21	chr4:3233786-3233836	HRPEpiC	eye:	n/a
22	chr4:3233774-3233824	HEEpiC	esophagus:	n/a
23	chr4:3235589-3235639	IMR90	lung:	fetal
24	chr4:3234933-3234983	PANC-1	pancreas:	n/a
25	chr4:3234417-3234467	HIPEpiC	eye:	n/a
26	chr4:3233865-3233915	PrEC	prostate:	n/a
27	chr4:3235295-3235345	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:3235319-3235369	HRCEpiC	kidney:	n/a
29	chr4:3233774-3233824	Caco-2	colon:	n/a
30	chr4:3234462-3234512	ECC-1	luminal epithelium:	n/a
31	chr4:3234933-3234983	HCT-116	colon:	n/a
32	chr4:3234417-3234467	NT2-D1	testis:	n/a
33	chr4:3234933-3234983	BE2_C	brain:	n/a
34	chr4:3235319-3235369	BE2_C	brain:	n/a
35	chr4:3234814-3234864	IMR90	lung:	fetal
36	chr4:3233774-3233824	AG04449	skin:	fetal
37	chr4:3235295-3235345	AG10803	skin:	n/a
38	chr4:3235589-3235639	K562	blood:	n/a
39	chr4:3233865-3233915	NH-A	brain:	n/a
40	chr4:3233865-3233915	LNCaP	prostate:	n/a
41	chr4:3234462-3234512	NHDF-neo	bronchial:	n/a
42	chr4:3233774-3233824	NB4	blood:	n/a
43	chr4:3234814-3234864	ProgFib	skin:	n/a
44	chr4:3234814-3234864	HUVEC	blood vessel:	n/a
45	chr4:3235000-3235050	HUVEC	blood vessel:	n/a
46	chr4:3235589-3235639	HNPCEpiC	eye:	n/a
47	chr4:3233774-3233824	GM06990	blood:	n/a
48	chr4:3233865-3233915	HNPCEpiC	eye:	n/a
49	chr4:3235589-3235639	GM12891	blood:	n/a
50	chr4:3235295-3235345	NHBE	bronchial:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3233193..3236137-chr4:3292325..3293850,2	MCF-7	breast:
2	chr4:3233021..3235441-chr4:3240275..3242127,2	K562	blood:
3	chr4:3231157..3234122-chr4:3467560..3470032,2	MCF-7	breast:
4	chr4:3225798..3228316-chr4:3230639..3233767,3	K562	blood:
5	chr4:3230258..3233203-chr4:3234240..3237131,3	K562	blood:
6	chr4:3230862..3233203-chr4:3234391..3237131,2	K562	blood:
7	chr4:3232769..3236525-chr4:3484558..3488114,4	MCF-7	breast:
8	chr4:3231863..3234034-chr4:3238136..3239944,2	MCF-7	breast:

No data

Variant related genes	Relation type
HTT	TF binding region
HTT	CpG island
ENSG00000175920	chromatin interactions
ENSG00000197386	chromatin interactions

Extended variants
information (count: 122 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:122 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs59588638	chr4:3233614-3233615	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573300661	chr4:3233668-3233669	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs540796360	chr4:3233690-3233691	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs538126808	chr4:3233704-3233705	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs554947060	chr4:3233720-3233721	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs574460991	chr4:3233721-3233722	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs34452575	chr4:3233735-3233736	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs540257788	chr4:3233737-3233738	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559958213	chr4:3233738-3233739	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs117525279	chr4:3233775-3233776	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs111921198	chr4:3233779-3233780	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs376120050	chr4:3233787-3233788	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs111387773	chr4:3233795-3233796	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs531834234	chr4:3233796-3233797	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs887031	chr4:3233844-3233845	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs188799847	chr4:3233856-3233857	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527653701	chr4:3233865-3233866	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs368716536	chr4:3233879-3233880	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543918965	chr4:3233895-3233896	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570812770	chr4:3233896-3233897	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs75194556	chr4:3233942-3233943	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs10021033	chr4:3233973-3233974	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs73074838	chr4:3233999-3234000	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs375986933	chr4:3234011-3234012	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551657137	chr4:3234050-3234051	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs111245352	chr4:3234062-3234063	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs566771170	chr4:3234106-3234107	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs181175747	chr4:3234150-3234151	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568377787	chr4:3234153-3234154	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79523063	chr4:3234158-3234159	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553731196	chr4:3234178-3234179	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs184045203	chr4:3234224-3234225	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10021254	chr4:3234241-3234242	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs567478746	chr4:3234245-3234246	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs555868780	chr4:3234283-3234284	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377020624	chr4:3234385-3234386	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs576215604	chr4:3234440-3234441	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs188341485	chr4:3234452-3234453	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs562018931	chr4:3234470-3234471	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs527992452	chr4:3234471-3234472	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs541027998	chr4:3234472-3234473	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs180707366	chr4:3234485-3234486	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs187189694	chr4:3234488-3234489	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs148816211	chr4:3234497-3234498	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs71608258	chr4:3234505-3234506	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs556237344	chr4:3234506-3234507	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs548426288	chr4:3234522-3234523	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs147996884	chr4:3234523-3234524	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs73074839	chr4:3234544-3234545	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs559227182	chr4:3234555-3234556	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3114600-3292400	Weak transcription	Right Atrium	heart
2	chr4:3145800-3239200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:3172400-3238800	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:3194000-3237600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:3196000-3242600	Strong transcription	Fetal Intestine Small	intestine
6	chr4:3201400-3238400	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:3204800-3246000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr4:3206000-3234800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:3206000-3244600	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr4:3206000-3246400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr4:3207600-3238600	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr4:3207600-3243600	Strong transcription	Primary B cells from peripheral blood	blood
13	chr4:3207600-3244000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:3207600-3244600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr4:3207600-3245400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:3207600-3246400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr4:3207800-3243200	Strong transcription	Sigmoid Colon	Sigmoid Colon
18	chr4:3207800-3243800	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr4:3207800-3244400	Strong transcription	Duodenum Mucosa	Duodenum
20	chr4:3207800-3245400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr4:3208000-3235800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr4:3208000-3243600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr4:3208200-3237400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr4:3208200-3239200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:3208200-3246400	Strong transcription	Fetal Thymus	thymus
26	chr4:3208400-3244800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:3210000-3244200	Strong transcription	Fetal Intestine Large	intestine
28	chr4:3210000-3245000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:3210000-3246600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:3210400-3247000	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr4:3211600-3246400	Strong transcription	Thymus	Thymus
32	chr4:3213400-3242600	Strong transcription	Ovary	ovary
33	chr4:3213400-3243400	Strong transcription	Dnd41	blood
34	chr4:3213400-3245600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:3213600-3238800	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr4:3213600-3245600	Strong transcription	Placenta Amnion	Placenta Amnion
37	chr4:3213800-3247600	Strong transcription	Primary T cells from cord blood	blood
38	chr4:3214000-3243400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr4:3221600-3238800	Weak transcription	Hela-S3	cervix
40	chr4:3222600-3241600	Strong transcription	Adipose Nuclei	Adipose
41	chr4:3223200-3243800	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr4:3223400-3247600	Strong transcription	Fetal Brain Female	brain
43	chr4:3224000-3236200	Weak transcription	Psoas Muscle	Psoas
44	chr4:3225200-3240800	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr4:3227000-3238200	Strong transcription	Primary B cells from cord blood	blood
46	chr4:3227200-3239200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:3228800-3237400	Strong transcription	HepG2	liver
48	chr4:3228800-3246600	Strong transcription	Liver	Liver
49	chr4:3229000-3243000	Strong transcription	Placenta	Placenta
50	chr4:3229000-3245400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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