Variant report

Variant	nsv433363
Chromosome Location	chr4:9480235-9586764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
3	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
4	BATF	chr4:9560693-9560899	GM12878	blood:	n/a	n/a
5	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
6	BATF	chr4:9481131-9481403	GM12878	blood:	n/a	n/a
7	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
8	BATF	chr4:9560631-9560870	GM12878	blood:	n/a	n/a
9	BATF	chr4:9481132-9481453	GM12878	blood:	n/a	n/a
10	BATF	chr4:9582818-9583030	GM12878	blood:	n/a	n/a
11	BATF	chr4:9582796-9583040	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
14	BHLHE40	chr4:9533811-9533913	K562	blood:	n/a	n/a
15	CCNT2	chr4:9533734-9533999	K562	blood:	n/a	n/a
16	CEBPB	chr4:9531399-9531602	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:9530664-9530884	K562	blood:	n/a	n/a
18	CEBPB	chr4:9530595-9530856	K562	blood:	n/a	n/a
19	CEBPB	chr4:9585906-9586106	HepG2	liver:	n/a	chr4:9585991-9586002
20	CEBPB	chr4:9530676-9530843	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr4:9533998-9534198	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr4:9533949-9534111	H1-hESC	embryonic stem cell:	n/a	chr4:9533994-9534004
23	CHD2	chr4:9533893-9534015	HepG2	liver:	n/a	chr4:9533994-9534004
24	CTCF	chr4:9533840-9533990	Caco-2	colon:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
25	CTCF	chr4:9533820-9533970	HEEpiC	esophagus:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
26	CTCF	chr4:9533840-9533990	HCPEpiC	choroid plexus:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
27	CTCF	chr4:9579220-9579370	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr4:9579560-9579710	GM12874	blood:	n/a	n/a
29	CTCF	chr4:9579605-9579778	GM12878	blood:	n/a	n/a
30	CTCF	chr4:9497133-9497477	GM12878	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
31	CTCF	chr4:9533800-9533950	HRE	kidney:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
32	CTCF	chr4:9497220-9497370	Caco-2	colon:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
33	CTCF	chr4:9533417-9533440	GM19238	blood:	n/a	n/a
34	CTCF	chr4:9579600-9579750	NB4	blood:	n/a	n/a
35	CTCF	chr4:9497209-9497342	SK-N-SH_RA	brain:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
36	CTCF	chr4:9497200-9497350	HPF	lung:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
37	CTCF	chr4:9533743-9534047	HepG2	liver:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
38	CTCF	chr4:9579540-9579690	GM12868	blood:	n/a	n/a
39	CTCF	chr4:9481140-9481410	GM06990	blood:	n/a	n/a
40	CTCF	chr4:9533840-9533990	HBMEC	blood vessel:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
41	CTCF	chr4:9497200-9497350	GM12875	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
42	CTCF	chr4:9497162-9497425	Gliobla	brain:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
43	CTCF	chr4:9497253-9497465	IMR90	lung:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
44	CTCF	chr4:9497121-9497415	H1-hESC	embryonic stem cell:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
45	CTCF	chr4:9579635-9579734	LNCaP	prostate:	n/a	n/a
46	CTCF	chr4:9497207-9497340	T-47D	breast:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
47	CTCF	chr4:9497240-9497390	GM12864	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
48	CTCF	chr4:9579580-9579730	GM12864	blood:	n/a	n/a
49	CTCF	chr4:9481074-9481548	K562	blood:	n/a	n/a
50	CTCF	chr4:9546131-9546279	MCF-7	breast:	n/a	chr4:9546245-9546261 chr4:9546244-9546262 chr4:9546239-9546260

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9533205-9533255	HCF	heart:	n/a
2	chr4:9492758-9492808	NB4	blood:	n/a
3	chr4:9507086-9507136	BE2_C	brain:	n/a
4	chr4:9493231-9493281	SKMC	muscle:	n/a
5	chr4:9533205-9533255	MCF10A-Er-Src	breast:	n/a
6	chr4:9533205-9533255	HRPEpiC	eye:	n/a
7	chr4:9533205-9533255	HCF	heart:	n/a
8	chr4:9492758-9492808	NB4	blood:	n/a
9	chr4:9507086-9507136	BE2_C	brain:	n/a
10	chr4:9493231-9493281	SKMC	muscle:	n/a
11	chr4:9533205-9533255	MCF10A-Er-Src	breast:	n/a
12	chr4:9533205-9533255	HRPEpiC	eye:	n/a
13	chr4:9507499-9507549	GM12891	blood:	n/a
14	chr4:9506681-9506731	NB4	blood:	n/a
15	chr4:9523635-9523685	NH-A	brain:	n/a
16	chr4:9495454-9495504	ovcar-3	ovarian:	n/a
17	chr4:9534313-9534363	AG09319	gingival:	n/a
18	chr4:9500174-9500224	PANC-1	pancreas:	n/a
19	chr4:9493231-9493281	GM06990	blood:	n/a
20	chr4:9533205-9533255	ProgFib	skin:	n/a
21	chr4:9505191-9505241	AoSMC	blood vessel:	n/a
22	chr4:9494211-9494261	SKMC	muscle:	n/a
23	chr4:9494396-9494446	HRCEpiC	kidney:	n/a
24	chr4:9495205-9495255	HIPEpiC	eye:	n/a
25	chr4:9537404-9537454	NHDF-neo	bronchial:	n/a
26	chr4:9523635-9523685	GM12891	blood:	n/a
27	chr4:9507499-9507549	U87	brain:	n/a
28	chr4:9534041-9534091	K562	blood:	n/a
29	chr4:9514864-9514914	HCM	heart:	n/a
30	chr4:9534041-9534091	T-47D	breast:	n/a
31	chr4:9534041-9534091	CMK	blood:	n/a
32	chr4:9514810-9514860	HCM	heart:	n/a
33	chr4:9485487-9485537	K562	blood:	n/a
34	chr4:9481822-9481872	PANC-1	pancreas:	n/a
35	chr4:9507086-9507136	GM12892	blood:	n/a
36	chr4:9485487-9485537	SK-N-SH_RA	brain:	n/a
37	chr4:9533948-9533998	SK-N-MC	brain:	n/a
38	chr4:9482074-9482124	BJ	skin:	n/a
39	chr4:9492758-9492808	HMEC	breast:	n/a
40	chr4:9533948-9533998	HL-60	blood:	n/a
41	chr4:9508254-9508304	AG09309	skin:	n/a
42	chr4:9481822-9481872	HMEC	breast:	n/a
43	chr4:9484735-9484785	GM12892	blood:	n/a
44	chr4:9499194-9499244	MCF-7	breast:	n/a
45	chr4:9509830-9509880	A549	lung:	n/a
46	chr4:9494907-9494957	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:9505698-9505748	GM12892	blood:	n/a
48	chr4:9508976-9509026	AG04450	lung:	fetal
49	chr4:9497357-9497407	NHBE	bronchial:	n/a
50	chr4:9493114-9493164	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:4147498..4148004-chr4:9497288..9497793,2	MCF-7	breast:
2	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
3	chr4:4147469..4148009-chr4:9497278..9497791,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1396O13.13.1-3	chr4:9555234-9555605	NONHSAT095137

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr4:9557878-9557899	MIMAT0005935_1

Variant related genes	Relation type
OR7E85P	TF binding region
ENSG00000249799	TF binding region
MIR548I2	TF binding region
ENSG00000249443	TF binding region
OR7E83P	TF binding region
ENSG00000244004	TF binding region
UNC93B7	TF binding region
ENSG00000242034	TF binding region
OR7E85P	CpG island
ENSG00000249799	CpG island
MIR548I2	CpG island
ENSG00000249443	CpG island
OR7E83P	CpG island
ENSG00000244004	CpG island
UNC93B7	CpG island
ENSG00000242034	CpG island

Extended variants
information (count: 6609 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6609 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375283576	chr4:9481078-9481079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs111939442	chr4:9481108-9481109	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs28762417	chr4:9481120-9481121	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs111238686	chr4:9481123-9481124	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs368972810	chr4:9481145-9481146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs112633292	chr4:9481159-9481160	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs188556763	chr4:9481173-9481174	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs75818536	chr4:9481192-9481193	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs373049125	chr4:9481213-9481214	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs531554750	chr4:9481266-9481267	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs112716332	chr4:9481292-9481293	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs191882484	chr4:9481305-9481306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs549760424	chr4:9481332-9481333	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs75708148	chr4:9481339-9481340	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs571559736	chr4:9481350-9481351	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs112056187	chr4:9481351-9481352	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs79694950	chr4:9481381-9481382	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs188355603	chr4:9481386-9481387	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs111517462	chr4:9481388-9481389	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs191195402	chr4:9481407-9481408	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs79879359	chr4:9481430-9481431	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2928888	chr4:9481494-9481495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs4974897	chr4:9481503-9481504	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
24	rs187736664	chr4:9481507-9481508	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113755311	chr4:9481528-9481529	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs555918594	chr4:9481610-9481611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs202232505	chr4:9481629-9481630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564304449	chr4:9481633-9481634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538443691	chr4:9481659-9481660	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs1871723	chr4:9481671-9481672	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs35087245	chr4:9481672-9481673	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs578228114	chr4:9481673-9481674	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs144064104	chr4:9481677-9481678	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs376117729	chr4:9481679-9481680	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs185706372	chr4:9481704-9481705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542283569	chr4:9481710-9481711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560650898	chr4:9481711-9481712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531399364	chr4:9481716-9481717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189837372	chr4:9481745-9481746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1871722	chr4:9481747-9481748	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs532475023	chr4:9481753-9481754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547729824	chr4:9481754-9481755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs193168351	chr4:9481779-9481780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529514696	chr4:9481807-9481808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527690875	chr4:9481822-9481823	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs551193536	chr4:9481823-9481824	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs549459737	chr4:9481828-9481829	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs567800615	chr4:9481847-9481848	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs538050389	chr4:9481867-9481868	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs184630155	chr4:9481872-9481873	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9481600-9482000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:9481600-9482000	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr4:9481800-9482000	Enhancers	Duodenum Mucosa	Duodenum
4	chr4:9484800-9503800	Weak transcription	Right Atrium	heart
5	chr4:9495800-9496800	Enhancers	Fetal Thymus	thymus
6	chr4:9496200-9496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr4:9496200-9496800	Enhancers	Thymus	Thymus
8	chr4:9496200-9497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:9496400-9496600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:9496400-9496800	Enhancers	Primary hematopoietic stem cells	blood
11	chr4:9496600-9499000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:9496800-9499600	Weak transcription	Primary hematopoietic stem cells	blood
13	chr4:9499000-9499200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
14	chr4:9499000-9499200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
15	chr4:9499000-9499600	Enhancers	Liver	Liver
16	chr4:9499000-9500400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
17	chr4:9499000-9500600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:9499200-9499400	Bivalent Enhancer	Fetal Thymus	thymus
19	chr4:9499200-9499600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:9499200-9499800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:9499200-9499800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
22	chr4:9499200-9500200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
23	chr4:9499200-9500200	Bivalent Enhancer	Adipose Nuclei	Adipose
24	chr4:9499200-9500400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
25	chr4:9499200-9500400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:9499200-9500600	Active TSS	H9 Cell Line	embryonic stem cell
27	chr4:9499200-9500600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
28	chr4:9499200-9500600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
29	chr4:9499200-9500600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
30	chr4:9499200-9500600	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr4:9499400-9499600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr4:9499400-9499600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr4:9499400-9499600	Active TSS	Brain Germinal Matrix	brain
34	chr4:9499400-9499600	Enhancers	Colonic Mucosa	Colon
35	chr4:9499400-9499600	Active TSS	Fetal Brain Female	brain
36	chr4:9499400-9499800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr4:9499400-9499800	Enhancers	Lung	lung
38	chr4:9499400-9500200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:9499400-9500400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
40	chr4:9499400-9500400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:9499400-9500600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
42	chr4:9499600-9499800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:9499600-9499800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:9499600-9499800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:9499600-9499800	Bivalent/Poised TSS	Fetal Intestine Large	intestine
46	chr4:9499600-9499800	Bivalent Enhancer	Fetal Lung	lung
47	chr4:9499600-9500000	Active TSS	Primary T cells from cord blood	blood
48	chr4:9499600-9500000	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr4:9499600-9500200	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:9499600-9500200	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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