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

TagContent
EnhancerAtlas ID
HS092-00027 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr1:1252950-1254670 
Target genes
Number: 48             
NameEnsembl ID
NOC2LENSG00000188976
SAMD11ENSG00000187634
RP11ENSG00000230699
PLEKHN1ENSG00000187583
C1orf170ENSG00000187642
HES4ENSG00000188290
ISG15ENSG00000187608
AGRNENSG00000188157
KLHL17ENSG00000187961
C1orf159ENSG00000131591
TNFRSF18ENSG00000186891
SDF4ENSG00000078808
B3GALT6ENSG00000176022
FAM132AENSG00000184163
RP5ENSG00000260179
UBE2J2ENSG00000160087
SCNN1DENSG00000162572
PUSL1ENSG00000169972
ACAP3ENSG00000131584
CPSF3LENSG00000127054
GLTPD1ENSG00000224051
TAS1R3ENSG00000169962
DVL1ENSG00000107404
MXRA8ENSG00000162576
AURKAIP1ENSG00000175756
CCNL2ENSG00000221978
RP4ENSG00000224870
MRPL20ENSG00000242485
ANKRD65ENSG00000235098
VWA1ENSG00000179403
ATAD3CENSG00000215915
ATAD3BENSG00000160072
ATAD3AENSG00000197785
TMEM240ENSG00000205090
AL645728.2ENSG00000215791
SSU72ENSG00000160075
AL645728.1ENSG00000215014
C1orf233ENSG00000228594
MIB2ENSG00000197530
MMP23BENSG00000189409
CDK11BENSG00000248333
SLC35E2BENSG00000189339
MMP23AENSG00000215914
CDK11AENSG00000008128
RP1ENSG00000227775
SLC35E2ENSG00000215790
NADKENSG00000008130
GNB1ENSG00000078369
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1886773chr11254436hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr1:1253765-1253776GGTGACTCATG+6.62
JUNDMA0491.1chr1:1253765-1253776GGTGACTCATG+6.02
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_06507chr1:1253891-1257912Brain_Hippocampus_Middle
SE_07598chr1:1253768-1255162Brain_Hippocampus_Middle_150
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr112536001254000
Number: 1             
IDChromosomeStartEnd
GH01I001317chr112528861255312
Enhancer Sequence
GAGGAGCAGG AACGGGGCAG AAACAACACT GGAAGAAACA TGATGAAGGC CTCAAGCCAC 60
AGATCCAAGA GGCCTCAAAC TCTAAACAGG CTGAGGATAC ATGTCAGCCC ATCAGAGCAC 120
AAGCACCAAA AACCAAGGCT CCTGCTCAGA CCCTACGGCT GCCCATGCCC AGAGACAGAA 180
CGTTGTTTGC AAAGTGCAGA GACAAAATAC TGTCAACCTA AAATCTTACA CACCTAAGGG 240
AAAAAAAGTC CTTTAAGAAC GAGGATAAAG TAAATCCATT TGCAGGCAAA TAAATTTTTT 300
TTTTTTGAGC CGGAGTCTCG CGTCTCGCTC TGTCTCCCAG GCTGGAGTGC AGTGGTGGGA 360
TCTTGGCTCA CTGCAAGCTC CGCCTCCCAG GTTCACGCCA TTCTCCTGCC TTTCAGCCTC 420
CCGAGTAGCT GGGACTGCAG GCGCCCGCAC CACGCCCAGC TAATTTTTTT GTATTTTGTT 480
TAGTAGAGAC AGGGTTTCAC CGTGTTAGCC AGGATGGTCT CGATCTCCTG ACCTCGTGAT 540
CCGCCTGTCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG CGCCTGGCCA 600
AGGCAAATAA AAATTGACAG AATTCAGCAC CAGCAGACCC ACACTCATAT TCTTCAGGCA 660
GAAGGCAAAT TATCCCAAGT AAAAAGTAGA AAAAATGCAG GAAGCCCAAC AAAAAGGATA 720
AATATATAAA TAAAACTAAG CAAATGTTGG TGTTACCAGG CATTAGAAAT GATGTCTTTC 780
TGGGTTTAAA ATGTACTGAG GGAGTTGCCA GGTGTGGTGA CTCATGCCTG TAATCCGAGC 840
ACTTTGAGAG GCTGAGGTGG GAGGATCCCT GGAGCCCAGC CCAGGAGTTC GAGAGCCTTA 900
GCAACACATA CCCATCTCTA CAAAAAATAC CAAAATAAAT TAGCTGGGCG TATGGGCACA 960
TGCTTGTAGT CCCAGCTACT TGGGAGGCCG AGGTGGGAGA TCACCTCAAC CCGGGAGGCC 1020
GAGGCTGCAG TGAGCCAAGA TCACACTCCA GCCTGGGTAA CAAAGTGAGA CACTGTCAAA 1080
AAAAAAAAAA AATTAAAGTT TCACAACAAA AAAGATAAAC ATACTTCATT TTGACAAGTT 1140
CAATCAGAAA ATTAAATGTT CCAAAATACA TAGGTACCTA ATATAGTTTC AAGAAATATA 1200
AAAGCAATAC CCAGAGATTC GAGTGAGACA CAGACAAACC CATAATCTTT GTCAGAAATG 1260
GAATTTCACC TGTCACTCGC TGATTTAACC TTCACTTCTT CCCTGACCCA CACCCAGAAC 1320
CAGGCACCCT CCAGAGCTGG CCCATCTCCC CTCCAGCCCC TGCCTCCCTG CCCGGCAACA 1380
CCCCGGGAGC TCCAGCGAGT CTCTGGCCGC TCCAAGCGCT CTGAGGGCAC CAGCCTGTCC 1440
CACTCTGGCC ATTTCAATGC CGCTCGGACA GAGCCTGGTG GGTTCATAAG CCGGTGCATA 1500
CCCCCACCCT GCACGTGCTC TCCCGGGTCG GCGCCCAGTC TGGTCTGGGA CCCGCATCCT 1560
CGCGCTGACG CCTCCTGGTG TCCCCACGGT GCTGGACGCA AGAGTGAGGT GGGGTGGGCT 1620
CACCCTGAGG CCCCAGCCTT CCAGAAACTG TGTAGAACGG GCGGAGGGCA TGGTTGGTGT 1680
GGGGGTGGGC AGTGACTGTG CCAGCTGTGG CCCTGGGAAC 1720