EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS192-13806 
Organism
Homo sapiens 
Tissue/cell
U2OS 
Coordinate
chr8:145535930-145537190 
Target genes
Number: 57             
NameEnsembl ID
7SKENSG00000221399
RP11ENSG00000254144
C8orf73ENSG00000204839
NAPRT1ENSG00000147813
TIGD5ENSG00000179886
ZNF707ENSG00000181135
MIR937ENSG00000216090
SCRIBENSG00000180900
PUF60ENSG00000179950
PLECENSG00000178209
GRINAENSG00000178719
PARP10ENSG00000178685
OPLAHENSG00000178814
EXOSC4ENSG00000178896
CTDENSG00000255224
GPAA1ENSG00000197858
CYC1ENSG00000179091
MAF1ENSG00000179632
SHARPINENSG00000179526
FAM203AENSG00000235173
TSSK5P1ENSG00000227473
HEATR7AENSG00000179832
SCXBENSG00000187786
AC145291.1ENSG00000204775
FAM203BENSG00000230567
SCXAENSG00000188686
BOP1ENSG00000170727
HSF1ENSG00000185122
GS1ENSG00000254690
DGAT1ENSG00000185000
SCRT1ENSG00000170616
SLC52A2ENSG00000185803
FBXL6ENSG00000182325
ADCK5ENSG00000173137
MIR939ENSG00000216133
CPSF1ENSG00000071894
SLC39A4ENSG00000147804
VPS28ENSG00000160948
AC084125.4ENSG00000232600
TONSLENSG00000160949
CYHR1ENSG00000187954
KIFC2ENSG00000167702
PPP1R16AENSG00000160972
GPTENSG00000167701
MFSD3ENSG00000167700
RECQL4ENSG00000160957
LRRC14ENSG00000160959
LRRC24ENSG00000254402
C8orf82ENSG00000213563
AC084125.1ENSG00000255681
AC084125.2ENSG00000256822
ARHGAP39ENSG00000147799
ZNF251ENSG00000198169
AF235103.1ENSG00000244307
RPL8ENSG00000161016
ZNF7ENSG00000147789
COMMD5ENSG00000170619
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs62530366chr8145536056hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SREBF1MA0595.1chr8:145536091-145536101ATCACCCCAC+6.02
TP53MA0106.3chr8:145536126-145536144GGCATGTCCGGACAGGCT-6.14
ZNF263MA0528.1chr8:145536353-145536374TTCCCCTGCCCCTCTTCCTCT-6.78
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_01158chr8:145536600-145537342Adrenal_Gland
SE_25128chr8:145536383-145538885Colon_Crypt_3
SE_34612chr8:145533968-145537348HCT-116
SE_52803chr8:145536386-145537366Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8145536067145536232
Number: 1             
IDChromosomeStartEnd
GH08I144310chr8145534265145540390
Enhancer Sequence
GTGAGTGCCG CCCACCCCTG GCCCCACCCA CAGCGCCTGG ACGCACAGCC CTGGGCTTCA 60
GCCCCGACTG TCCCAGTGGA CTGAGCAGGG CAGCTGGCGA GGCAGGACCC TACCCCCAAC 120
CTCGGAGCTC GGGGCTGGGG AGGGAGACAG GTGCCAGCCA GATCACCCCA CAGTCCCAAA 180
CGCCACAGAA GCCACGGGCA TGTCCGGACA GGCTGCCGGG CCCTGCTCTC AGCCACCCCT 240
CCTGCTGCCG CCACCCTCGC CACAGGCCAC GGGCCCTGGC AGGTCGTGCT GCCCAGACAC 300
ATGGCAGGAG ATGGTGAGCA GGGCCGGCCT CCACACCCCC AGCCCCTGCC TGCAATGGGG 360
GCTCTTGTTT TTGTATCTTG CAGTTTGGCT CGCACTCCAC AGATGTCTAG GGTCGCCCGC 420
CTCTTCCCCT GCCCCTCTTC CTCTCCGCAT GGCCAAGTCC AGCCAGGGTT AGCGCTGACC 480
CCACTGGGGA GGGAGGAGGG CTCTGCCAGC GCTCGGGCCC TCCCACACAG CCGTGGACCA 540
GACCCAGCCT GGCCGGGCAT GAGCGTCGGG CCTGGGCGGC AGCAGCCGAG ACCCCTCTGT 600
GGCGGGGGCT CAGTGTCGTC ATGGCTCCCC TGGCCACGGG CCTGTGGTCA TTGCCTGTGA 660
CAGGGATGAC AGGGACAGGC CTCCCTGCTC TGGCACGGCC TCTGGTGTTG GCAGGATCCA 720
GACTGCGGTG CTGACTGCAC TTCCTGTCAG GCAGGGTCTC CAGGGCACCT CTGGGACCCA 780
GCCTGGCTGT CCGTCCCATA GCCCAGGTGT GCCCTGTGGC CTAGGGCTTT CTTGGTCACA 840
GCCACCAGAC CGTGGGTCTC ATCCCCACAG CAGCACCAGG GCAGGGACTG AGCCACCCAC 900
ACACTGAGCA GAGCCCCACC TGTTTTCCCA GTGCAACGGG AAACCTCACC AACCCTGAAC 960
ACTGAAATCC CTGATCCTTG TGCTGGAGCT GAATACGCCC CTTGTCTCCT GGGTCCACTG 1020
CCACCAAGGC CCCCAGGCCC TCATGGCAAA GGGATGCCCA GCATAGGCCC AGCCGCACCC 1080
CTGCAGGGCA CAGAGCCTCC ACTGCCTTCC AGGCCGTCCT CGAATGCGCT GCCCCCTCCA 1140
GCCTGTGCAG GCGTACACGG GGGTGCAGCC TGGGGGGTAC AGTCAAGGGG AGCCCTTCTC 1200
CCACAGGAGG GCATTGGGGT GTGGGGCCTG GGGCACTGGT TCAGGTACCG CCTTATCCCG 1260