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

TagContent
EnhancerAtlas ID
HS060-06044 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr11:64682780-64684430 
Target genes
Number: 38             
NameEnsembl ID
SLC22A12ENSG00000197891
NRXN2ENSG00000110076
RASGRP2ENSG00000068831
PYGMENSG00000068976
SF1ENSG00000168066
MAP4K2ENSG00000168067
MEN1ENSG00000133895
CDC42BPGENSG00000171219
AP001187.11ENSG00000230835
EHD1ENSG00000110047
AP001187.1ENSG00000203400
AP001187.9ENSG00000229719
ATG2AENSG00000110046
PPP2R5BENSG00000068971
GPHA2ENSG00000149735
C11orf85ENSG00000168070
BATF2ENSG00000168062
ARL2ENSG00000213465
SNX15ENSG00000110025
SAC3D1ENSG00000168061
NAALADL1ENSG00000168060
CDCA5ENSG00000146670
ZFPL1ENSG00000162300
C11orf2ENSG00000149823
AP003068.6ENSG00000187066
AP003068.9ENSG00000254501
TM7SF2ENSG00000149809
AP003068.12ENSG00000255173
ZNHIT2ENSG00000174276
MRPL49ENSG00000149792
FAUENSG00000149806
SYVN1ENSG00000162298
AP003068.18ENSG00000255200
CAPN1ENSG00000014216
AP003068.23ENSG00000254614
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
FRMD8ENSG00000126391
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs188954228chr1164682925hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr11:64683973-64683988GGGGTCAAGAGGTCA+8.07
Nr2f6MA0677.1chr11:64683329-64683343AAGGTTAGAGGTCA+6.06
RARAMA0729.1chr11:64683973-64683991GGGGTCAAGAGGTCAGGG+6.56
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr116468287064682981
chr116468286364683400
chr116468340064683600
Enhancer Sequence
GGGCCTCAGT AAACTGGTTG GATCCAAGAA TAAAAAAGCA CATGGCAGAG CAGATGGGAG 60
TCCAAATTCC TCACCCAGAG ACCCACAGCT CGGGAAACTG AGGCCTAGAG ACAGGACTAA 120
TCTAGTCACC CAGTATACAA CAGGGACTGA GACTGGGATG CGGGCCTCTT TCTTTTCATG 180
CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG 240
CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG CCTGCATTCC ACCAGGGCCC 300
TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG 360
GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG TGGTTCATGC CTATAATCTC 420
AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA 480
CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG 540
GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC CAGAATTCAC AGACAGCAGG 600
CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC TACCCCACAT TTGCTCACCA 660
GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA 720
GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT GCTGCTCTGG ACCTGGTGGA 780
TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG 840
TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG ACCTTACACC TCTTGGCCTC 900
CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA TCTCCCCACC TTTCCTCCAG 960
GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG TGGGAGATGT AGGTGGGGGC 1020
CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC TCTCCCAAAA GCAGGAAGTA 1080
GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT ACTGACGTAC TGACGCGGTT 1140
GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG GGCTCAGGAC CGTGGGGTCA 1200
AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG CTCCGGACCC CTACCAGCTT 1260
CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG GCCCAGCTCA GTTCCTACGC 1320
TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT TAACTCAGCC CCCAAACTCG 1380
ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC TCTCCAGCCT CAGTTTCTCC 1440
TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG AACTGAAGAG 1500
GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT CCCCTGGCCT CTCTACGCCC 1560
GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT CAGGTCGCTG CGCTCCCACC 1620
CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1650