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

TagContent
EnhancerAtlas ID
HS108-07742 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr11:64682460-64684430 
Target genes
Number: 47             
NameEnsembl ID
GPR137ENSG00000173264
BADENSG00000002330
ESRRAENSG00000173153
TRMT112ENSG00000173113
PRDX5ENSG00000126432
NRXN2ENSG00000110076
RASGRP2ENSG00000068831
PYGMENSG00000068976
SF1ENSG00000168066
MAP4K2ENSG00000168067
MEN1ENSG00000133895
CDC42BPGENSG00000171219
AP001187.11ENSG00000230835
EHD1ENSG00000110047
AP001187.1ENSG00000203400
MIR192ENSG00000207648
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
HIGD1AP10ENSG00000254455
U2ENSG00000222477
SPDYCENSG00000204710
AP003068.18ENSG00000255200
CAPN1ENSG00000014216
AP003068.23ENSG00000254614
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
DPF2ENSG00000133884
NEAT1ENSG00000245532
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs188954228chr1164682925hg19
TF binding sites/motifs
Number: 8             
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
RREB1MA0073.1chr11:64682613-64682633CCCACCACCAACCCCAAACA+6.16
RREB1MA0073.1chr11:64682610-64682630CCCCCCACCACCAACCCCAA+6.93
RREB1MA0073.1chr11:64682607-64682627CCCCCCCCCACCACCAACCC+7.34
TCF7L2MA0523.1chr11:64682551-64682565AGAGTTCAAAGGGA+6.28
ZNF740MA0753.2chr11:64682605-64682618CCCCCCCCCCCAC+6.92
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr116468287064682981
chr116468286364683400
chr116468340064683600
Enhancer Sequence
GCGCTGGTAG AAGGTGGTGT GTTGCAGGCA CAGGACAACA TGGGCACATG TATGGCAGAG 60
TCCAGAATAC CCATGTTCAC CCTGGATGAG CAGAGTTCAA AGGGACAGTG TCCAAGAGAG 120
GGGCTGACCT AATGCCAGAT GGGACCCCCC CCCCCCACCA CCAACCCCAA ACACCTAGTG 180
TAGCTGTGCC TCTCTGTGAG GCACAAGGCT GAGCCCCTGG CTAAAATGTC CATGCTGGAG 240
TTGTACCCCT GCCAACCTGG AAGCTCCTGG AGGGCTGTAC CCCACCTGCC TCCCCCGTCA 300
CCCCAGGTGC CACCCAGAAA GGGCCTCAGT AAACTGGTTG GATCCAAGAA TAAAAAAGCA 360
CATGGCAGAG CAGATGGGAG TCCAAATTCC TCACCCAGAG ACCCACAGCT CGGGAAACTG 420
AGGCCTAGAG ACAGGACTAA TCTAGTCACC CAGTATACAA CAGGGACTGA GACTGGGATG 480
CGGGCCTCTT TCTTTTCATG CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC 540
TTCAAGGCGG GGCCTGCAGG CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG 600
CCTGCATTCC ACCAGGGCCC TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC 660
AGGAGTAGGG GCGTTTTCTG GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG 720
TGGTTCATGC CTATAATCTC AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG 780
TTCAAGGCTA GCCTGGGCAA CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA 840
GCCTAGAGAC GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC 900
CAGAATTCAC AGACAGCAGG CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC 960
TACCCCACAT TTGCTCACCA GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA 1020
TTAGCAGCCC CCTGAGTCCA GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT 1080
GCTGCTCTGG ACCTGGTGGA TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC 1140
TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG 1200
ACCTTACACC TCTTGGCCTC CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA 1260
TCTCCCCACC TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG 1320
TGGGAGATGT AGGTGGGGGC CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC 1380
TCTCCCAAAA GCAGGAAGTA GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT 1440
ACTGACGTAC TGACGCGGTT GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG 1500
GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG 1560
CTCCGGACCC CTACCAGCTT CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG 1620
GCCCAGCTCA GTTCCTACGC TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT 1680
TAACTCAGCC CCCAAACTCG ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC 1740
TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC 1800
TCTGGTAAGG AACTGAAGAG GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT 1860
CCCCTGGCCT CTCTACGCCC GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT 1920
CAGGTCGCTG CGCTCCCACC CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1970