Variant report

Variant	rs4417181
Chromosome Location	chr10:90967093-90967094
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr10:90967060-90967850	ECC-1	luminal epithelium:	n/a	n/a
2	ZNF263	chr10:90966529-90968646	HEK293-T-REx	kidney:	n/a	n/a
3	TBP	chr10:90966988-90967245	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr10:90966214-90967345	H1-hESC	embryonic stem cell:	n/a	n/a
5	USF1	chr10:90966988-90967475	SK-N-SH_RA	brain:	n/a	n/a
6	E2F4	chr10:90967076-90967264	MCF10A-Er-Src	breast:	n/a	n/a
7	CEBPB	chr10:90967078-90967537	A549	lung:	n/a	n/a
8	POLR2A	chr10:90966800-90967369	ProgFib	skin:	n/a	n/a
9	BACH1	chr10:90966612-90967905	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr10:90966766-90967491	PFSK-1	brain:	n/a	n/a
11	CEBPB	chr10:90967011-90967556	IMR90	lung:	n/a	n/a
12	RAD21	chr10:90966614-90967293	SK-N-SH_RA	brain:	n/a	n/a
13	ELF1	chr10:90966410-90967179	GM12878	blood:	n/a	n/a
14	TAF1	chr10:90966948-90967269	PFSK-1	brain:	n/a	n/a
15	SIN3AK20	chr10:90966929-90967258	SK-N-SH	brain:	n/a	n/a
16	ATF2	chr10:90967074-90967622	H1-hESC	embryonic stem cell:	n/a	n/a
17	STAT3	chr10:90967026-90967537	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr10:90966703-90967515	U87	brain:	n/a	n/a
19	MAX	chr10:90966226-90967526	H1-hESC	embryonic stem cell:	n/a	n/a
20	SUZ12	chr10:90966287-90967907	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr10:90966761-90967365	U87	brain:	n/a	n/a
22	STAT3	chr10:90967025-90967394	MCF10A-Er-Src	breast:	n/a	n/a
23	MAZ	chr10:90966597-90967921	IMR90	lung:	n/a	n/a
24	JUND	chr10:90967089-90967276	K562	blood:	n/a	n/a
25	STAT3	chr10:90966979-90967327	MCF10A-Er-Src	breast:	n/a	n/a
26	MAZ	chr10:90967001-90967161	HepG2	liver:	n/a	n/a
27	USF1	chr10:90966977-90967214	H1-hESC	embryonic stem cell:	n/a	n/a
28	MAX	chr10:90966955-90967849	SK-N-SH	brain:	n/a	n/a
29	KAP1	chr10:90967073-90967603	HEK293	kidney:	n/a	n/a
30	POLR2A	chr10:90967070-90968096	H1-neurons	neurons:	n/a	n/a
31	POLR2A	chr10:90966656-90967167	Gliobla	brain:	n/a	n/a
32	POLR2A	chr10:90966697-90967515	U87	brain:	n/a	n/a
33	MAX	chr10:90966269-90967653	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr10:90967029-90967431	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr10:90966724-90968174	H1-neurons	neurons:	n/a	n/a
36	E2F6	chr10:90966052-90967348	H1-hESC	embryonic stem cell:	n/a	n/a
37	FOXP2	chr10:90966437-90967271	PFSK-1	brain:	n/a	n/a
38	MAX	chr10:90966153-90967546	H1-hESC	embryonic stem cell:	n/a	n/a
39	SIN3A	chr10:90966852-90968132	H1-hESC	embryonic stem cell:	n/a	chr10:90967717-90967726 chr10:90967710-90967723

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90967052-90967102	SKMC	muscle:	n/a
2	chr10:90967052-90967102	SAEC	small airway:	n/a
3	chr10:90967052-90967102	ECC-1	luminal epithelium:	n/a
4	chr10:90967052-90967102	HCM	heart:	n/a
5	chr10:90967052-90967102	GM06990	blood:	n/a
6	chr10:90967052-90967102	HRPEpiC	eye:	n/a
7	chr10:90967052-90967102	HAEpiC	amniotic membrane:	n/a
8	chr10:90967052-90967102	Hepatocyte	liver:	n/a
9	chr10:90967052-90967102	NHDF-neo	bronchial:	n/a
10	chr10:90967052-90967102	AG09309	skin:	n/a
11	chr10:90967052-90967102	RPTEC	kidney:	n/a
12	chr10:90967052-90967102	ovcar-3	ovarian:	n/a
13	chr10:90967052-90967102	GM19239	blood:	n/a
14	chr10:90967052-90967102	SK-N-MC	brain:	n/a
15	chr10:90967052-90967102	H1-hESC	embryonic stem cell:	embryo
16	chr10:90967052-90967102	K562	blood:	n/a
17	chr10:90967052-90967102	ProgFib	skin:	n/a
18	chr10:90967052-90967102	HRE	kidney:	n/a
19	chr10:90967052-90967102	AG10803	skin:	n/a
20	chr10:90967052-90967102	SK-N-SH_RA	brain:	n/a
21	chr10:90967052-90967102	NH-A	brain:	n/a
22	chr10:90967052-90967102	T-47D	breast:	n/a
23	chr10:90967052-90967102	HCPEpiC	choroid plexus:	n/a
24	chr10:90967052-90967102	GM12891	blood:	n/a
25	chr10:90967052-90967102	HUVEC	blood vessel:	n/a
26	chr10:90967052-90967102	HRCEpiC	kidney:	n/a
27	chr10:90967052-90967102	Hela-S3	cervix:	n/a
28	chr10:90967052-90967102	PFSK-1	brain:	n/a
29	chr10:90967052-90967102	HEK293	kidney:	embryo
30	chr10:90967052-90967102	HepG2	liver:	n/a
31	chr10:90967052-90967102	BJ	skin:	n/a
32	chr10:90967052-90967102	CMK	blood:	n/a
33	chr10:90967052-90967102	AG04450	lung:	fetal
34	chr10:90967052-90967102	BE2_C	brain:	n/a
35	chr10:90967052-90967102	IMR90	lung:	fetal
36	chr10:90967052-90967102	Caco-2	colon:	n/a
37	chr10:90967052-90967102	HPAEpiC	pulmonary alveolar:	n/a
38	chr10:90967052-90967102	LNCaP	prostate:	n/a
39	chr10:90967052-90967102	PANC-1	pancreas:	n/a
40	chr10:90967052-90967102	U87	brain:	n/a
41	chr10:90967052-90967102	HIPEpiC	eye:	n/a
42	chr10:90967052-90967102	HNPCEpiC	eye:	n/a
43	chr10:90967052-90967102	SK-N-SH	brain:	n/a
44	chr10:90967052-90967102	AoSMC	blood vessel:	n/a
45	chr10:90967052-90967102	HCF	heart:	n/a
46	chr10:90967052-90967102	HL-60	blood:	n/a
47	chr10:90967052-90967102	HMEC	breast:	n/a
48	chr10:90967052-90967102	Jurkat	blood:	n/a
49	chr10:90967052-90967102	HCT-116	colon:	n/a
50	chr10:90967052-90967102	AG09319	gingival:	n/a

No data

Variant related genes	Relation type
CH25H	TF binding region
CH25H	CpG island

Extended variants
information (count: 69 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10430718	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10509567	0.94[AMR][1000 genomes]
rs10509568	0.83[JPT][hapmap]
rs10887920	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10887921	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10887922	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10887923	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10887924	0.83[ASN][1000 genomes]
rs10887925	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10887926	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10887927	0.94[AMR][1000 genomes]
rs10887928	0.94[AMR][1000 genomes]
rs10887929	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10887932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11203009	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11203011	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11203014	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11203017	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11203018	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11203024	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11203025	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11203030	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11203031	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11203032	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11203033	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12217507	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12219735	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12250945	0.83[ASN][1000 genomes]
rs17117088	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17117124	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17117126	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1977501	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2154255	0.94[AMR][1000 genomes]
rs2211599	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2863216	0.94[AMR][1000 genomes]
rs2902445	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3802657	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3802658	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3923282	0.91[AMR][1000 genomes]
rs4078488	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4294494	1.00[AFR][1000 genomes]
rs4399251	0.94[AMR][1000 genomes]
rs4511206	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4617498	0.94[AMR][1000 genomes]
rs4933494	0.91[AMR][1000 genomes]
rs61853069	0.83[ASN][1000 genomes]
rs61853072	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7074977	0.83[ASN][1000 genomes]
rs7076185	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7098394	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7477966	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7896174	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7902290	0.83[ASN][1000 genomes]
rs7922269	0.89[JPT][hapmap]
rs9651424	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9651495	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	esv2758235	chr10:90835064-91017486	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2759775	chr10:90835064-91017486	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
6	nsv517170	chr10:90931602-90975207	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv437127	chr10:90940003-90968103	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv467422	chr10:90940687-90975207	Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv467423	chr10:90940687-90975207	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv551858	chr10:90940687-90975207	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv1038123	chr10:90954417-90992129	Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv1040280	chr10:90962032-90979093	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv1042428	chr10:90962252-90977164	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4417181	GRID1	cis	parietal	SCAN
rs4417181	LIPA	cis	cerebellum	SCAN
rs4417181	GRID1	cis	cerebellum	SCAN

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90964800-90967400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr10:90965600-90968400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
3	chr10:90966000-90968400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr10:90966200-90967200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr10:90966200-90967200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr10:90966200-90967200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
7	chr10:90966200-90967200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
8	chr10:90966200-90967200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
9	chr10:90966200-90967200	Flanking Active TSS	Lung	lung
10	chr10:90966200-90967200	Flanking Active TSS	NHLF	lung
11	chr10:90966200-90967400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr10:90966200-90967400	Flanking Bivalent TSS/Enh	Dnd41	blood
13	chr10:90966200-90967600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
14	chr10:90966200-90967600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
15	chr10:90966200-90968000	Active TSS	Brain Angular Gyrus	brain
16	chr10:90966200-90968200	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr10:90966200-90968200	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
18	chr10:90966200-90968200	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
19	chr10:90966200-90968200	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
20	chr10:90966200-90968200	Bivalent/Poised TSS	A549	lung
21	chr10:90966200-90968400	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
22	chr10:90966200-90968400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
23	chr10:90966200-90968400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr10:90966200-90968400	Flanking Active TSS	Adipose Nuclei	Adipose
25	chr10:90966200-90968400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
26	chr10:90966200-90968600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
27	chr10:90966400-90967200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
28	chr10:90966400-90967200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
29	chr10:90966400-90967200	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
30	chr10:90966400-90967200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:90966400-90967200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr10:90966400-90967200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
33	chr10:90966400-90967200	Flanking Active TSS	Pancreas	Pancrea
34	chr10:90966400-90967400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
35	chr10:90966400-90967600	Active TSS	Aorta	Aorta
36	chr10:90966400-90967600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
37	chr10:90966400-90967600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
38	chr10:90966400-90967600	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
39	chr10:90966400-90968000	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr10:90966400-90968000	Active TSS	Ovary	ovary
41	chr10:90966400-90968200	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
42	chr10:90966400-90968200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
43	chr10:90966400-90968200	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
44	chr10:90966400-90968200	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
45	chr10:90966400-90968200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
46	chr10:90966400-90968200	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
47	chr10:90966400-90968400	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
48	chr10:90966400-90968400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
49	chr10:90966400-90968400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
50	chr10:90966400-90968400	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood

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