Variant report

Variant	rs4970987
Chromosome Location	chr1:150949682-150949683
allele	C/T
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	BHLHE40	chr1:150949195-150950106	K562	blood:	n/a	n/a
2	ETS1	chr1:150949621-150950098	K562	blood:	n/a	chr1:150949995-150950002 chr1:150949991-150950006 chr1:150949699-150949712 chr1:150949991-150950002 chr1:150949989-150950003
3	MAZ	chr1:150949345-150950151	K562	blood:	n/a	n/a
4	MYC	chr1:150949387-150950151	K562	blood:	n/a	n/a
5	POLR2A	chr1:150949639-150950281	Hela-S3	cervix:	n/a	n/a
6	HEY1	chr1:150949661-150950248	HepG2	liver:	n/a	n/a
7	MAX	chr1:150949068-150950119	K562	blood:	n/a	n/a
8	HEY1	chr1:150949128-150950179	K562	blood:	n/a	n/a
9	POLR2A	chr1:150948639-150950133	K562	blood:	n/a	n/a
10	SPI1	chr1:150949488-150950308	HL-60	blood:	n/a	chr1:150949996-150950003 chr1:150949699-150949712
11	SP1	chr1:150949170-150950418	HCT-116	colon:	n/a	chr1:150949692-150949705 chr1:150949950-150949960 chr1:150949950-150949960
12	BCLAF1	chr1:150949514-150950125	K562	blood:	n/a	n/a
13	JUN	chr1:150949372-150950424	K562	blood:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949987-150949997 chr1:150950040-150950054
14	FOSL1	chr1:150949348-150950328	HCT-116	colon:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949987-150949997 chr1:150950040-150950054
15	JUND	chr1:150949481-150950426	HCT-116	colon:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949986-150949997 chr1:150949987-150949997 chr1:150950040-150950054
16	POLR2A	chr1:150949600-150950259	SK-N-SH	brain:	n/a	n/a
17	IRF1	chr1:150948650-150950171	K562	blood:	n/a	chr1:150949992-150950001 chr1:150949947-150949961
18	SP1	chr1:150949534-150950412	A549	lung:	n/a	chr1:150949692-150949705 chr1:150949950-150949960 chr1:150949950-150949960
19	SP1	chr1:150949642-150950221	H1-hESC	embryonic stem cell:	n/a	chr1:150949692-150949705 chr1:150949950-150949960 chr1:150949950-150949960
20	GTF2B	chr1:150949550-150949979	K562	blood:	n/a	n/a
21	GATA2	chr1:150949481-150949973	K562	blood:	n/a	chr1:150949745-150949761 chr1:150949750-150949757 chr1:150949750-150949757 chr1:150949739-150949756 chr1:150949748-150949758 chr1:150949743-150949764 chr1:150949748-150949757 chr1:150949750-150949757
22	POLR2A	chr1:150949401-150950218	K562	blood:	n/a	n/a
23	TBL1XR1	chr1:150949244-150950095	K562	blood:	n/a	n/a
24	REST	chr1:150949551-150949856	K562	blood:	n/a	n/a
25	CCNT2	chr1:150949295-150950324	K562	blood:	n/a	chr1:150949739-150949759
26	PML	chr1:150949308-150950059	K562	blood:	n/a	n/a
27	MAX	chr1:150949651-150950295	A549	lung:	n/a	n/a
28	TEAD4	chr1:150949106-150950150	K562	blood:	n/a	n/a
29	ETS1	chr1:150949659-150950237	A549	lung:	n/a	chr1:150949995-150950002 chr1:150949991-150950006 chr1:150949699-150949712 chr1:150949991-150950002 chr1:150949989-150950003
30	MYC	chr1:150949646-150950203	NB4	blood:	n/a	n/a
31	MAX	chr1:150949658-150950255	SK-N-SH	brain:	n/a	n/a
32	POLR2A	chr1:150948648-150950161	K562	blood:	n/a	n/a
33	MXI1	chr1:150949631-150949948	K562	blood:	n/a	n/a
34	TCF12	chr1:150949616-150950297	ECC-1	luminal epithelium:	n/a	n/a
35	HDAC2	chr1:150949413-150950157	K562	blood:	n/a	chr1:150949444-150949453 chr1:150949666-150949680 chr1:150949672-150949686 chr1:150949670-150949684 chr1:150949671-150949685
36	STAT5A	chr1:150949501-150949969	K562	blood:	n/a	n/a
37	EGR1	chr1:150949605-150949893	K562	blood:	n/a	n/a
38	POLR2A	chr1:150949492-150950275	U87	brain:	n/a	n/a
39	UBTF	chr1:150949512-150950022	K562	blood:	n/a	n/a
40	SIX5	chr1:150949280-150950423	A549	lung:	n/a	chr1:150949584-150949593
41	TAF1	chr1:150949675-150949916	K562	blood:	n/a	n/a
42	RFX5	chr1:150949499-150949764	K562	blood:	n/a	n/a
43	FOSL2	chr1:150949631-150950335	SK-N-SH	brain:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949985-150949996 chr1:150949987-150949997 chr1:150950040-150950054
44	TRIM28	chr1:150949549-150949867	K562	blood:	n/a	n/a
45	CEBPD	chr1:150949388-150950176	K562	blood:	n/a	n/a
46	ZNF143	chr1:150949595-150949998	K562	blood:	n/a	chr1:150949954-150949969
47	POLR2A	chr1:150949218-150950275	U87	brain:	n/a	n/a
48	POLR2A	chr1:150949582-150950239	H1-hESC	embryonic stem cell:	n/a	n/a
49	JUN	chr1:150949461-150950112	K562	blood:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949987-150949997 chr1:150950040-150950054
50	POLR2A	chr1:150949322-150950258	HCT-116	colon:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:150550324..150553500-chr1:150948263..150951593,4	MCF-7	breast:
2	chr1:150949558..150951518-chr1:150957213..150958786,2	K562	blood:
3	chr1:150942078..150949693-chr1:150976791..150984782,24	MCF-7	breast:
4	chr1:150897410..150900366-chr1:150947492..150952156,4	K562	blood:
5	chr1:150949543..150951625-chr11:11620473..11621993,2	MCF-7	breast:
6	chr1:150949479..150950097-chr20:56964168..56964788,2	Hela-S3	cervix:
7	chr1:150948646..150951124-chr1:150967629..150969757,2	K562	blood:
8	chr1:150948448..150951342-chr1:151016605..151018874,2	K562	blood:
9	chr1:150948791..150950437-chr17:56735372..56737821,2	MCF-7	breast:
10	chr1:150948040..150949859-chr1:150959159..150961414,2	K562	blood:
11	chr1:150949418..150950356-chr17:39844321..39845262,2	Hela-S3	cervix:
12	chr1:150520324..150522575-chr1:150949260..150951135,2	K562	blood:
13	chr1:150892976..150894840-chr1:150949265..150951717,2	K562	blood:
14	chr1:150205150..150208917-chr1:150946080..150950396,4	MCF-7	breast:
15	chr1:149859214..149861702-chr1:150947048..150949834,2	MCF-7	breast:

Variant related genes	Relation type
ANXA9	TF binding region
CERS2	TF binding region
ENSG00000184270	Chromatin interaction
ENSG00000143409	Chromatin interaction
ENSG00000163141	Chromatin interaction
ENSG00000143401	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000143363	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000124164	Chromatin interaction
ENSG00000225996	Chromatin interaction
ENSG00000173812	Chromatin interaction
ENSG00000143382	Chromatin interaction
ENSG00000143384	Chromatin interaction
ENSG00000143379	Chromatin interaction

Extended variants
information (count: 88 )
Associated
traits (count: 28 )

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10305704	1.00[CEU][hapmap]
rs10305711	0.95[CEU][hapmap]
rs10305714	1.00[CEU][hapmap]
rs10399947	0.80[EUR][1000 genomes]
rs10888394	0.87[CEU][hapmap]
rs10888397	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10888398	0.87[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs11204739	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11204742	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11204743	0.85[ASN][1000 genomes]
rs11204747	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11204748	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11204749	0.90[CHB][hapmap];0.85[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11204750	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11552229	1.00[CEU][hapmap]
rs11579736	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11581757	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11583707	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11589886	0.83[ASN][1000 genomes]
rs12059949	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12067685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12085336	0.87[CEU][hapmap]
rs12090215	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12096831	0.87[CHB][hapmap];0.82[JPT][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12097963	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12141871	0.85[CHB][hapmap]
rs12145224	0.86[CHB][hapmap]
rs12405726	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12409208	1.00[CEU][hapmap];0.87[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12410394	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12410869	0.87[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap]
rs12562939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1546376	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1889740	0.87[CEU][hapmap]
rs1889741	0.87[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs1972060	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2004903	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2124952	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2228099	0.87[CEU][hapmap]
rs2256355	0.87[CEU][hapmap]
rs2271076	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2272214	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2280627	0.88[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2864873	0.87[CEU][hapmap]
rs2864882	0.82[ASN][1000 genomes]
rs2867296	0.85[EUR][1000 genomes]
rs34985895	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3768013	0.87[CEU][hapmap]
rs3768015	1.00[CEU][hapmap]
rs3768016	1.00[CEU][hapmap]
rs3843843	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3849279	0.87[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4451553	0.95[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4509581	0.83[CEU][hapmap]
rs4970928	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4970929	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4970930	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4970931	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4970982	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4970984	0.83[ASN][1000 genomes]
rs4970985	0.83[ASN][1000 genomes]
rs4970986	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4970988	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59024312	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6587542	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6658066	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6660845	0.80[EUR][1000 genomes]
rs6669855	0.80[EUR][1000 genomes]
rs6677420	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs66847267	0.82[ASN][1000 genomes]
rs72704679	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72704682	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72704685	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7518156	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs752376	0.87[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7528773	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7532045	0.87[CEU][hapmap]
rs7548516	0.91[CHB][hapmap];0.91[YRI][hapmap];0.88[ASN][1000 genomes]
rs7556451	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7556661	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8444	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs897815	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9661876	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001897	chr1:150743271-151241600	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv535158	chr1:150743271-151241600	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
3	nsv1008496	chr1:150845827-150970656	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
4	nsv522317	chr1:150933723-150974162	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv522840	chr1:150933723-151347746	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	169 gene(s)	inside rSNPs	diseases

mRNA abundance (count:28)

SNP	Gene	Cis/trans	Tissue	Source
rs4970987	GOLPH3L	cis	Skin Sun Exposed Lower leg	GTEx
rs4970987	RP11-316M1.12	cis	Whole Blood	GTEx
rs4970987	HORMAD1	cis	Esophagus Mucosa	GTEx
rs4970987	HORMAD1	cis	Skin Sun Exposed Lower leg	GTEx
rs4970987	RP11-316M1.12	cis	Artery Tibial	GTEx
rs4970987	HORMAD1	cis	normal skin	skin_eQTL
rs4970987	RP11-316M1.12	cis	Heart Left Ventricle	GTEx
rs4970987	RP11-316M1.12	cis	lung	GTEx
rs4970987	ARNT	cis	normal skin	skin_eQTL
rs4970987	CTSS	cis	Lymphoblastoid	GTEx
rs4970987	RP11-316M1.12	cis	Adipose Subcutaneous	GTEx
rs4970987	CTSS	Cis_1M	lymphoblastoid	RTeQTL
rs4970987	RP11-316M1.12	cis	Esophagus Muscularis	GTEx
rs4970987	RP11-316M1.12	cis	Nerve Tibial	GTEx
rs4970987	CTSK	Cis_1M	lymphoblastoid	RTeQTL
rs4970987	HORMAD1	cis	Nerve Tibial	GTEx
rs4970987	RP11-316M1.12	cis	Esophagus Mucosa	GTEx
rs4970987	RP11-316M1.12	cis	Muscle Skeletal	GTEx
rs4970987	HORMAD1	cis	lesional skin	skin_eQTL
rs4970987	RP11-316M1.12	cis	Thyroid	GTEx
rs4970987	HORMAD1	cis	Adipose Subcutaneous	GTEx
rs4970987	CTSS	cis	Thyroid	GTEx
rs4970987	ARNT	Cis_1M	lymphoblastoid	RTeQTL
rs4970987	RNU6-1042P	cis	Esophagus Mucosa	GTEx
rs4970987	HORMAD1	cis	uninvolved skin	skin_eQTL
rs4970987	CTSS	cis	multi-tissue	Pritchard
rs4970987	GOLPH3L	cis	Nerve Tibial	GTEx
rs4970987	RP11-316M1.12	cis	Artery Aorta	GTEx

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150947600-150949800	Weak transcription	Gastric	stomach
2	chr1:150947800-150949800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:150947800-150950400	Enhancers	Stomach Mucosa	stomach
4	chr1:150947800-150950400	Flanking Active TSS	K562	blood
5	chr1:150947800-150950400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr1:150948000-150949800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:150948000-150949800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:150948000-150949800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:150948000-150949800	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr1:150948000-150949800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:150948000-150949800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr1:150948000-150949800	Enhancers	Liver	Liver
13	chr1:150948000-150949800	Weak transcription	Esophagus	oesophagus
14	chr1:150948000-150949800	Weak transcription	Left Ventricle	heart
15	chr1:150948000-150949800	Weak transcription	Pancreas	Pancrea
16	chr1:150948000-150949800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr1:150948000-150949800	Weak transcription	Right Atrium	heart
18	chr1:150948000-150949800	Weak transcription	Right Ventricle	heart
19	chr1:150948000-150949800	Enhancers	Spleen	Spleen
20	chr1:150948000-150950200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:150948000-150950200	Enhancers	Fetal Muscle Leg	muscle
22	chr1:150948000-150950200	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr1:150948000-150950400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:150948000-150950400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:150948000-150950400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr1:150948000-150950400	Enhancers	NHEK	skin
27	chr1:150948000-150950600	Enhancers	Fetal Thymus	thymus
28	chr1:150948000-150951600	Enhancers	Primary T cells fromperipheralblood	blood
29	chr1:150948000-150951600	Weak transcription	Colonic Mucosa	Colon
30	chr1:150948000-150951600	Enhancers	Fetal Intestine Large	intestine
31	chr1:150948000-150951600	Weak transcription	Fetal Kidney	kidney
32	chr1:150948000-150951600	Weak transcription	Ovary	ovary
33	chr1:150948000-150951800	Weak transcription	Psoas Muscle	Psoas
34	chr1:150948000-150952600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr1:150948000-150952600	Enhancers	Fetal Intestine Small	intestine
36	chr1:150948200-150949800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:150948200-150949800	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr1:150948200-150949800	Weak transcription	Dnd41	blood
39	chr1:150948200-150949800	Weak transcription	GM12878-XiMat	blood
40	chr1:150948200-150950000	Enhancers	Brain Hippocampus Middle	brain
41	chr1:150948200-150950000	Weak transcription	Colon Smooth Muscle	Colon
42	chr1:150948200-150950200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:150948200-150950400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:150948200-150950600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:150948200-150951400	Weak transcription	Fetal Lung	lung
46	chr1:150948200-150951600	Enhancers	Primary T cells from cord blood	blood
47	chr1:150948200-150951800	Weak transcription	Brain Germinal Matrix	brain
48	chr1:150948200-150952000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr1:150948400-150950200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr1:150948400-150950200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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