Variant report

Variant	esv3371193
Chromosome Location	chr4:2962104-2963452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:55 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:2963128-2963328	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:2962087-2962384	HepG2	liver:	n/a	n/a
3	BRCA1	chr4:2963194-2963383	HepG2	liver:	n/a	n/a
4	CEBPB	chr4:2962145-2962326	K562	blood:	n/a	n/a
5	CHD2	chr4:2963290-2963449	K562	blood:	n/a	n/a
6	CTCF	chr4:2963296-2963382	GM19239	blood:	n/a	n/a
7	CTCF	chr4:2963120-2963270	BE2_C	brain:	n/a	n/a
8	FOS	chr4:2963387-2963613	MCF10A-Er-Src	breast:	n/a	n/a
9	HDAC2	chr4:2962866-2963280	K562	blood:	n/a	n/a
10	JUN	chr4:2963038-2966039	K562	blood:	n/a	chr4:2965875-2965884
11	KAP1	chr4:2963204-2963990	U2OS	brain:	n/a	n/a
12	MAX	chr4:2963069-2963467	K562	blood:	n/a	n/a
13	MAX	chr4:2963179-2963409	HepG2	liver:	n/a	n/a
14	MAX	chr4:2963092-2966134	NB4	blood:	n/a	chr4:2965876-2965886 chr4:2965246-2965255
15	MAZ	chr4:2963305-2963559	HepG2	liver:	n/a	n/a
16	MAZ	chr4:2963249-2963319	K562	blood:	n/a	n/a
17	MTA3	chr4:2963307-2964119	GM12878	blood:	n/a	n/a
18	MXI1	chr4:2963102-2963530	HepG2	liver:	n/a	n/a
19	MXI1	chr4:2963144-2963530	K562	blood:	n/a	n/a
20	MXI1	chr4:2963015-2966472	SK-N-SH	brain:	n/a	n/a
21	MYC	chr4:2963421-2963447	K562	blood:	n/a	n/a
22	MYC	chr4:2963164-2965858	K562	blood:	n/a	chr4:2965246-2965255
23	MYC	chr4:2963304-2963404	HepG2	liver:	n/a	n/a
24	MYC	chr4:2963362-2963944	K562	blood:	n/a	n/a
25	MYC	chr4:2963149-2963532	NB4	blood:	n/a	n/a
26	MYC	chr4:2963372-2965382	MCF10A-Er-Src	breast:	n/a	chr4:2965246-2965255
27	POLR2A	chr4:2963187-2963801	GM12891	blood:	n/a	n/a
28	POLR2A	chr4:2963302-2965861	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr4:2963223-2963413	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr4:2963077-2963753	K562	blood:	n/a	n/a
31	POLR2A	chr4:2963286-2963423	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr4:2963047-2966632	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr4:2963024-2963995	GM12892	blood:	n/a	n/a
34	POLR2A	chr4:2963100-2963330	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr4:2963071-2963498	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr4:2963071-2964319	GM12892	blood:	n/a	n/a
37	POLR2A	chr4:2963307-2963369	Gliobla	brain:	n/a	n/a
38	POLR2A	chr4:2963063-2964245	GM12878	blood:	n/a	n/a
39	POLR2A	chr4:2963280-2963305	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr4:2963169-2963437	HepG2	liver:	n/a	n/a
41	POLR2A	chr4:2961976-2962422	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr4:2963067-2963471	HL-60	blood:	n/a	n/a
43	POLR2A	chr4:2963214-2963399	GM12891	blood:	n/a	n/a
44	POLR2A	chr4:2963220-2963408	K562	blood:	n/a	n/a
45	POLR2A	chr4:2963182-2963444	HepG2	liver:	n/a	n/a
46	POLR2A	chr4:2963144-2963636	GM12878	blood:	n/a	n/a
47	POLR2A	chr4:2963027-2963897	SK-N-MC	brain:	n/a	n/a
48	SIN3AK20	chr4:2963158-2963424	K562	blood:	n/a	n/a
49	SREBP1	chr4:2963426-2965715	GM12878	blood:	n/a	n/a
50	UBTF	chr4:2963139-2966263	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2963264-2963314	HMEC	breast:	n/a
2	chr4:2963264-2963314	NT2-D1	testis:	n/a
3	chr4:2963264-2963314	AG04449	skin:	fetal
4	chr4:2963264-2963314	SK-N-SH	brain:	n/a
5	chr4:2963261-2963311	GM19239	blood:	n/a
6	chr4:2963264-2963314	HRE	kidney:	n/a
7	chr4:2963264-2963314	MCF-7	breast:	n/a
8	chr4:2963264-2963314	AG04450	lung:	fetal
9	chr4:2963264-2963314	IMR90	lung:	fetal
10	chr4:2963264-2963314	BJ	skin:	n/a
11	chr4:2963264-2963314	HIPEpiC	eye:	n/a
12	chr4:2963264-2963314	Hela-S3	cervix:	n/a
13	chr4:2963261-2963311	NHBE	bronchial:	n/a
14	chr4:2963261-2963311	AG10803	skin:	n/a
15	chr4:2963261-2963311	SK-N-SH	brain:	n/a
16	chr4:2963261-2963311	SK-N-SH_RA	brain:	n/a
17	chr4:2963264-2963314	NHDF-neo	bronchial:	n/a
18	chr4:2963261-2963311	GM12891	blood:	n/a
19	chr4:2963264-2963314	HNPCEpiC	eye:	n/a
20	chr4:2963261-2963311	AG09309	skin:	n/a
21	chr4:2963264-2963314	NH-A	brain:	n/a
22	chr4:2963264-2963314	AG10803	skin:	n/a
23	chr4:2963264-2963314	ECC-1	luminal epithelium:	n/a
24	chr4:2963261-2963311	GM06990	blood:	n/a
25	chr4:2963261-2963311	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:2963264-2963314	AG09309	skin:	n/a
27	chr4:2963261-2963311	ECC-1	luminal epithelium:	n/a
28	chr4:2963264-2963314	GM19239	blood:	n/a
29	chr4:2963264-2963314	A549	lung:	n/a
30	chr4:2963264-2963314	RPTEC	kidney:	n/a
31	chr4:2963261-2963311	ProgFib	skin:	n/a
32	chr4:2963264-2963314	HAEpiC	amniotic membrane:	n/a
33	chr4:2963264-2963314	HRPEpiC	eye:	n/a
34	chr4:2963264-2963314	Jurkat	blood:	n/a
35	chr4:2963261-2963311	Hepatocyte	liver:	n/a
36	chr4:2963261-2963311	NHDF-neo	bronchial:	n/a
37	chr4:2963261-2963311	HIPEpiC	eye:	n/a
38	chr4:2963264-2963314	PrEC	prostate:	n/a
39	chr4:2963261-2963311	HEK293	kidney:	embryo
40	chr4:2963261-2963311	PANC-1	pancreas:	n/a
41	chr4:2963261-2963311	NB4	blood:	n/a
42	chr4:2963264-2963314	Caco-2	colon:	n/a
43	chr4:2963261-2963311	HNPCEpiC	eye:	n/a
44	chr4:2963261-2963311	PrEC	prostate:	n/a
45	chr4:2963264-2963314	AoSMC	blood vessel:	n/a
46	chr4:2963261-2963311	HL-60	blood:	n/a
47	chr4:2963261-2963311	AG04450	lung:	fetal
48	chr4:2963264-2963314	GM12878	blood:	n/a
49	chr4:2963264-2963314	BE2_C	brain:	n/a
50	chr4:2963261-2963311	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:2937577..2939558-chr4:2961657..2964358,2	MCF-7	breast:
2	chr4:2795940..2798085-chr4:2962031..2964351,2	MCF-7	breast:
3	chr4:2959980..2962211-chr4:2969909..2971816,3	MCF-7	breast:
4	chr4:2756517..2759780-chr4:2963075..2966456,5	K562	blood:
5	chr4:2948388..2950164-chr4:2962609..2964597,2	MCF-7	breast:
6	chr4:2963409..2964972-chr4:2976613..2978274,2	MCF-7	breast:
7	chr4:2936328..2940860-chr4:2961848..2966602,8	K562	blood:
8	chr4:2960088..2962960-chr4:3074155..3076323,2	MCF-7	breast:
9	chr4:2756517..2759604-chr4:2963075..2966301,5	K562	blood:
10	chr4:2961872..2963731-chr4:3064483..3066913,2	K562	blood:
11	chr4:2948727..2950755-chr4:2959506..2963214,4	K562	blood:
12	chr4:2935142..2937747-chr4:2962615..2966345,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADD1-1	chr4:2963081-2963465	ENSG00000249673

No data

Variant related genes	Relation type
GRK4	TF binding region
GRK4	CpG island
ENSG00000109736	chromatin interactions
ENSG00000249673	chromatin interactions
ENSG00000168884	chromatin interactions
ENSG00000251075	chromatin interactions
ENSG00000125388	chromatin interactions
PABPC4	miRNA target sites

Extended variants
information (count: 117 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549997938	chr4:2962134-2962135	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs372381427	chr4:2962182-2962183	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs570166282	chr4:2962188-2962189	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs376781734	chr4:2962200-2962201	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs549126493	chr4:2962215-2962216	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs111447144	chr4:2962250-2962251	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs534693029	chr4:2962264-2962265	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs185693171	chr4:2962322-2962323	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs571604625	chr4:2962352-2962353	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs537248753	chr4:2962385-2962386	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs554790253	chr4:2962387-2962388	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs201789208	chr4:2962390-2962391	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs188972117	chr4:2962393-2962394	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs535504733	chr4:2962395-2962396	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs193045879	chr4:2962403-2962404	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs572043942	chr4:2962408-2962409	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs369723482	chr4:2962415-2962416	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs9686032	chr4:2962421-2962422	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
19	rs184392633	chr4:2962422-2962423	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs34508820	chr4:2962425-2962426	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs150954762	chr4:2962432-2962433	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
22	rs188780457	chr4:2962438-2962439	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs35681707	chr4:2962452-2962453	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
24	rs60925145	chr4:2962469-2962470	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs189326415	chr4:2962477-2962478	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs55845482	chr4:2962483-2962484	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
27	rs549489088	chr4:2962484-2962485	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs187314276	chr4:2962510-2962511	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs559988055	chr4:2962514-2962515	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs71180106	chr4:2962517-2962518	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs559583601	chr4:2962521-2962522	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs528532945	chr4:2962522-2962523	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs55690564	chr4:2962525-2962526	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs71297515	chr4:2962552-2962553	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs192374806	chr4:2962553-2962554	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs551437249	chr4:2962554-2962555	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs56007901	chr4:2962573-2962574	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs56333630	chr4:2962581-2962582	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs55972473	chr4:2962583-2962584	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs56079275	chr4:2962591-2962592	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs55977300	chr4:2962598-2962599	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs56229498	chr4:2962600-2962601	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs200345387	chr4:2962604-2962605	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs55766937	chr4:2962626-2962627	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs55695620	chr4:2962634-2962635	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs201291765	chr4:2962639-2962640	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs56227807	chr4:2962648-2962649	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs58492071	chr4:2962656-2962657	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs556496370	chr4:2962672-2962673	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs58634172	chr4:2962678-2962679	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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

Chromatin state (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2938200-2962200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:2938400-2962200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr4:2939200-2963200	Weak transcription	Fetal Heart	heart
4	chr4:2939400-2962200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr4:2940000-2962200	Strong transcription	Primary B cells from peripheral blood	blood
6	chr4:2948800-2963200	Strong transcription	Fetal Intestine Small	intestine
7	chr4:2953600-2963200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr4:2954400-2962400	Strong transcription	A549	lung
9	chr4:2956000-2963200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:2957600-2962200	Strong transcription	Fetal Intestine Large	intestine
11	chr4:2958200-2962200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:2958200-2963200	Weak transcription	Stomach Mucosa	stomach
13	chr4:2958400-2963000	Strong transcription	K562	blood
14	chr4:2958400-2963200	Weak transcription	Brain Substantia Nigra	brain
15	chr4:2958400-2963200	Weak transcription	Fetal Brain Male	brain
16	chr4:2958400-2963200	Weak transcription	Fetal Kidney	kidney
17	chr4:2958600-2962400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:2958800-2963200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:2958800-2963200	Weak transcription	Colon Smooth Muscle	Colon
20	chr4:2959200-2962600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr4:2959200-2963000	Weak transcription	Brain Germinal Matrix	brain
22	chr4:2959200-2964400	Weak transcription	Aorta	Aorta
23	chr4:2959400-2963000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:2959400-2963000	Weak transcription	Pancreas	Pancrea
25	chr4:2959400-2963000	Weak transcription	Small Intestine	intestine
26	chr4:2959400-2963200	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr4:2959400-2963600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr4:2959600-2963000	Weak transcription	Brain Anterior Caudate	brain
29	chr4:2959600-2963000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr4:2959600-2963200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:2959600-2963200	Weak transcription	Colonic Mucosa	Colon
32	chr4:2959800-2963000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr4:2959800-2963200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr4:2959800-2963200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:2959800-2963200	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr4:2959800-2963200	Weak transcription	Rectal Smooth Muscle	rectum
37	chr4:2959800-2963400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr4:2960000-2963000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr4:2960000-2963200	Weak transcription	Brain Angular Gyrus	brain
40	chr4:2960000-2963200	Weak transcription	Esophagus	oesophagus
41	chr4:2960200-2962200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:2960200-2962200	Genic enhancers	Primary T cells fromperipheralblood	blood
43	chr4:2960400-2962400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:2960400-2963200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr4:2960400-2963200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr4:2960400-2963200	Weak transcription	Brain Cingulate Gyrus	brain
47	chr4:2960600-2962200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
48	chr4:2960600-2962400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:2960600-2963000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr4:2960600-2963000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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