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

TagContent
EnhancerAtlas ID
HS095-00027 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr1:1217700-1218850 
Target genes
Number: 47             
NameEnsembl ID
NOC2LENSG00000188976
SAMD11ENSG00000187634
RP11ENSG00000234711
PLEKHN1ENSG00000187583
C1orf170ENSG00000187642
HES4ENSG00000188290
ISG15ENSG00000187608
AGRNENSG00000188157
KLHL17ENSG00000187961
FAM41CENSG00000230368
RNF223ENSG00000237330
C1orf159ENSG00000131591
TTLL10ENSG00000162571
TNFRSF18ENSG00000186891
SDF4ENSG00000078808
B3GALT6ENSG00000176022
FAM132AENSG00000184163
RP5ENSG00000260179
UBE2J2ENSG00000160087
SCNN1DENSG00000162572
PUSL1ENSG00000169972
ACAP3ENSG00000131584
CPSF3LENSG00000127054
GLTPD1ENSG00000224051
TAS1R3ENSG00000169962
DVL1ENSG00000107404
MXRA8ENSG00000162576
AURKAIP1ENSG00000175756
CCNL2ENSG00000221978
RP4ENSG00000224870
MRPL20ENSG00000242485
ANKRD65ENSG00000235098
TMEM88BENSG00000205116
VWA1ENSG00000179403
ATAD3CENSG00000215915
ATAD3BENSG00000160072
ATAD3AENSG00000197785
TMEM240ENSG00000205090
SSU72ENSG00000160075
AL645728.1ENSG00000215014
AL645728.3ENSG00000236684
C1orf233ENSG00000228594
MIB2ENSG00000197530
MMP23BENSG00000189409
CDK11BENSG00000248333
SLC35E2BENSG00000189339
MMP23AENSG00000215914
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr1:1218126-1218147AATCACTTTCTTTTTTTTTTT+6.52
RREB1MA0073.1chr1:1218462-1218482TTGGTGTGTGTGGTGTGGGT-6.01
ZfxMA0146.2chr1:1218375-1218389CCCGCCTCGGCCTC+6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr112180031218119
Number: 1             
IDChromosomeStartEnd
GH01I001280chr112160931218144
Enhancer Sequence
TGACCTCACC CTCCTCAGAG CCATGGCTCT GCTGCTGGAC CCTGTGGGGC TGGGCTCCCC 60
CAGCCAAGCC CAGGGACCCA GCACCACTTG GGGCAGGATG TCAGGAACAC AGAGCCTACC 120
CTTCCAACCT GGGCCCGGCT CGGGTCTGGT CATTTGGGAC AGTGAGGCCA CCTGGATATC 180
TAGGGTCCCA CAGTAGACAG GGATGGGGTG GTCCTGGGGG ACAGGGACAC CTGCCTTCCA 240
CACAACCGCA CTGGGGCTGA AGACGCCAGC CTGGGAGACT GTGATTTGGA CCCTGACAGT 300
AGCATGTGGT CTTAGCATGT GTGAGGTCTT AGCGTGTGTG GTCTTAGTGT GTGTGAGGTC 360
GTAGCGTGTG TGAGGTATTA GCATACGTGT GTGGTCTTAG CATGTGTGGG GTCTTAGTGT 420
GTTGTGAATC ACTTTCTTTT TTTTTTTTTT GAGACGGAGT CTTGCTCTGT CGCCCAGGCT 480
GGAGTGCAGT GGCACGATCT CGGCTCACTG CAAGCTCCGC CTCCTGGGTT CACACCATTC 540
TCCTGCCTCA GCCTCCCCAG TAGCTGGGAC TACAGGTGCC TGCCACCGCG CCCACCTAAT 600
TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCGTGTTAG GCAGGATGGT CTCAAACTCC 660
TGACCTTGTG ATCCGCCCGC CTCGGCCTCC CAAAGTGCTG AGATTACAGG CGTGAGCCAC 720
CGCGCCTGGT GGTCGTGAGT CACTTCCATG TGTGCCAGCA TCTTGGTGTG TGTGGTGTGG 780
GTGTGGACTG AAAGTCTTAG TGTGTGGCGC GTCATCTTAG TGTGTGGTGT GGTTGGTGGC 840
AGCTATAGTG TCCAGCAGGG AGGGCGAGCC CCTGTGCCTA CTCGGGGGAG CAGGTGCCTT 900
CTCCACACCC AGACCCTTGG TGTTCCCACA TTAGCACCTG TCCCAATGGC TGGGCGGCTG 960
GTCCCGAGAG ACACTGGATC TGGGAGCTGA GGTCCCCACC CAGTGTCTGT CAGCCAGGGA 1020
AGGGAGGGAG TGCTGGGAGC CCACCACGGC CCCGGATCTG AGTTCCAGGA GCTGGCAGAG 1080
AAAGATGGGG CTTCTGGGCC GGGCACGGTG GCTCACGCCT GTAATCCTAG CACTTCGGGA 1140
GGCTAAGGCG 1150