Variant report

Variant	rs10789464
Chromosome Location	chr1:45959102-45959103
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	CTCF	chr1:45958858-45959109	MCF-7	breast:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
2	RAD21	chr1:45958857-45959124	K562	blood:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
3	CTCF	chr1:45958419-45959383	SK-N-SH	brain:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
4	RAD21	chr1:45958800-45959154	K562	blood:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
5	RAD21	chr1:45958730-45959173	GM12878	blood:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
6	CTCF	chr1:45958755-45959170	HepG2	liver:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
7	CTCF	chr1:45958848-45959132	HUVEC	blood vessel:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
8	RAD21	chr1:45958471-45959439	SK-N-SH	brain:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
9	RAD21	chr1:45958705-45959231	ECC-1	luminal epithelium:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
10	USF2	chr1:45958921-45959134	Hela-S3	cervix:	n/a	n/a
11	RAD21	chr1:45958740-45959240	A549	lung:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
12	CTCF	chr1:45958590-45959220	A549	lung:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
13	CTCF	chr1:45958847-45959126	Lung_OC	lung:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
14	RAD21	chr1:45958692-45959152	H1-hESC	embryonic stem cell:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
15	RAD21	chr1:45958774-45959165	H1-hESC	embryonic stem cell:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
16	RFX5	chr1:45958807-45959126	Hela-S3	cervix:	n/a	n/a
17	ZNF143	chr1:45958830-45959119	K562	blood:	n/a	n/a
18	JUND	chr1:45958844-45959114	K562	blood:	n/a	n/a
19	CTCF	chr1:45958980-45959130	WI-38	lung:	n/a	n/a
20	FOXM1	chr1:45958721-45959202	GM12878	blood:	n/a	n/a
21	SMC3	chr1:45958748-45959179	Hela-S3	cervix:	n/a	chr1:45958977-45958987 chr1:45958979-45958993 chr1:45958977-45958991
22	SMC3	chr1:45958785-45959173	HepG2	liver:	n/a	chr1:45958977-45958987 chr1:45958979-45958993 chr1:45958977-45958991
23	RUNX3	chr1:45958768-45959191	GM12878	blood:	n/a	n/a
24	RAD21	chr1:45958719-45959190	Hela-S3	cervix:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
25	CTCF	chr1:45958960-45959110	NHEK	skin:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
26	RAD21	chr1:45958775-45959161	IMR90	lung:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
27	RAD21	chr1:45958727-45959224	A549	lung:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
28	RAD21	chr1:45958665-45959244	MCF-7	breast:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
29	MAZ	chr1:45958822-45959120	K562	blood:	n/a	n/a
30	CTCF	chr1:45958553-45959343	HCT-116	colon:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
31	CTCF	chr1:45958761-45959178	GM12878	blood:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
32	RAD21	chr1:45958715-45959240	ECC-1	luminal epithelium:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
33	CTCF	chr1:45958719-45959142	K562	blood:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
34	CTCF	chr1:45958845-45959112	K562	blood:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
35	RAD21	chr1:45958537-45959360	HCT-116	colon:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
36	MYC	chr1:45958814-45959108	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr1:45958835-45959143	A549	lung:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
38	CTCF	chr1:45958783-45959181	K562	blood:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
39	CTCF	chr1:45958746-45959118	H1-hESC	embryonic stem cell:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
40	CTCF	chr1:45958704-45959255	MCF-7	breast:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
41	RAD21	chr1:45958607-45959320	HCT-116	colon:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
42	SMC3	chr1:45958696-45959193	GM12878	blood:	n/a	chr1:45958977-45958987 chr1:45958979-45958993 chr1:45958977-45958991
43	CTCF	chr1:45958776-45959123	K562	blood:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
44	CTCF	chr1:45958852-45959106	GM12878	blood:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
45	CTCF	chr1:45958870-45959108	LNCaP	prostate:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
46	EBF1	chr1:45958847-45959193	GM12878	blood:	n/a	chr1:45959098-45959109 chr1:45959064-45959075
47	CTCF	chr1:45958680-45959185	IMR90	lung:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990
48	RAD21	chr1:45958738-45959138	H1-hESC	embryonic stem cell:	n/a	chr1:45958976-45958989 chr1:45958975-45958987 chr1:45958977-45958987 chr1:45958973-45958992
49	EBF1	chr1:45958904-45959254	GM12878	blood:	n/a	chr1:45959098-45959109 chr1:45959064-45959075
50	CTCF	chr1:45958846-45959126	Medullo	brain:	n/a	chr1:45958970-45958991 chr1:45958978-45958988 chr1:45958975-45958993 chr1:45958977-45958990

No.	Distal block	Cell Line	Cell type
1	chr1:45824288..45826262-chr1:45958481..45959657,14	K562	blood:
2	chr1:45825417..45826256-chr1:45958518..45959473,3	MCF-7	breast:
3	chr1:45819408..45822200-chr1:45957439..45959167,2	K562	blood:
4	chr1:45256108..45258642-chr1:45958911..45960479,2	K562	blood:
5	chr1:45956512..45959436-chr1:45986078..45988665,3	MCF-7	breast:
6	chr1:45194608..45195631-chr1:45958489..45959461,3	K562	blood:
7	chr1:45805035..45807382-chr1:45957250..45960213,2	MCF-7	breast:
8	chr1:45954905..45960579-chr1:45960652..45966878,10	K562	blood:
9	chr1:45957125..45959472-chr1:46015494..46017725,2	K562	blood:
10	chr1:45804184..45806968-chr1:45958652..45961269,2	K562	blood:
11	chr1:45479563..45480379-chr1:45959012..45959647,2	K562	blood:

Variant related genes	Relation type
TESK2	TF binding region
ENSG00000117450	Chromatin interaction
ENSG00000132763	Chromatin interaction
ENSG00000132781	Chromatin interaction
ENSG00000238945	Chromatin interaction
ENSG00000236624	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000117448	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1006216	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1007858	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10890327	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10890330	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11211108	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11211111	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11211117	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11211118	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11211123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11211124	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11211128	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12029322	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12037201	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12042903	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12046816	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12066142	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12067642	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12097497	0.83[EUR][1000 genomes]
rs12410493	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12564806	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1494812	0.83[EUR][1000 genomes]
rs1771551	0.81[EUR][1000 genomes]
rs1826691	0.82[EUR][1000 genomes]
rs2055145	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2088100	0.83[EUR][1000 genomes]
rs28555082	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2883968	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34673142	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3790582	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3790583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4633317	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4660855	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4660858	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4660863	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5015340	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55642258	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61788261	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61788262	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs61788281	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61788285	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61788336	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61788356	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61791369	0.81[EUR][1000 genomes]
rs67683090	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs713358	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7528573	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7531253	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs781226	0.80[EUR][1000 genomes]
rs781230	0.81[EUR][1000 genomes]
rs781232	0.81[EUR][1000 genomes]
rs868351	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9727262	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9729395	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	esv1795802	chr1:45819489-46009818	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	esv1831217	chr1:45819489-46009818	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
4	nsv530016	chr1:45868543-46069020	Flanking Active TSS Genic enhancers Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
5	nsv829726	chr1:45897581-46103186	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
6	nsv529631	chr1:45905936-46335246	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	207 gene(s)	inside rSNPs	diseases
7	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
8	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs10789464	MMACHC	cis	multi-tissue	Pritchard
rs10789464	PRDX1	cis	Thyroid	GTEx
rs10789464	C2orf49	trans	lymphoblastoid	RTeQTL
rs10789464	MUTYH	Cis_1M	lymphoblastoid	RTeQTL
rs10789464	TESK2	cis	Whole Blood	GTEx

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45956800-45964600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:45956800-45964800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr1:45956800-45964800	Weak transcription	Spleen	Spleen
4	chr1:45956800-45965000	Weak transcription	Gastric	stomach
5	chr1:45956800-45974000	Weak transcription	Small Intestine	intestine
6	chr1:45957000-45962600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:45957000-45964200	Weak transcription	Pancreas	Pancrea
8	chr1:45957000-45964400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:45957000-45964600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:45957000-45964800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:45957200-45961800	Weak transcription	Lung	lung
12	chr1:45957200-45964200	Weak transcription	K562	blood
13	chr1:45957400-45959800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr1:45957400-45964000	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:45957400-45964600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:45957400-45965200	Weak transcription	HSMM	muscle
17	chr1:45957600-45959200	Enhancers	Primary B cells from peripheral blood	blood
18	chr1:45957600-45959600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:45957600-45960800	Weak transcription	Primary T cells from cord blood	blood
20	chr1:45957600-45961800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:45957600-45962200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:45957600-45964000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr1:45957600-45964000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr1:45957600-45964200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:45957600-45964200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr1:45957600-45964200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:45957600-45964400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr1:45957600-45964600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr1:45957600-45964600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr1:45957600-45964600	Weak transcription	Ovary	ovary
31	chr1:45957600-45964600	Weak transcription	Thymus	Thymus
32	chr1:45957600-45964600	Weak transcription	Osteobl	bone
33	chr1:45957600-45964800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:45957600-45964800	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr1:45957600-45964800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr1:45957600-45965000	Weak transcription	Psoas Muscle	Psoas
37	chr1:45957800-45959800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr1:45957800-45960200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:45957800-45960200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr1:45957800-45961800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:45957800-45961800	Weak transcription	Esophagus	oesophagus
42	chr1:45957800-45961800	Weak transcription	Left Ventricle	heart
43	chr1:45957800-45961800	Weak transcription	Right Atrium	heart
44	chr1:45957800-45961800	Weak transcription	NHEK	skin
45	chr1:45957800-45962000	Weak transcription	Placenta	Placenta
46	chr1:45957800-45962200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr1:45957800-45962200	Weak transcription	Fetal Stomach	stomach
48	chr1:45957800-45964000	Weak transcription	Liver	Liver
49	chr1:45957800-45964000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr1:45957800-45964000	Weak transcription	Brain Substantia Nigra	brain

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