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

TagContent
EnhancerAtlas ID
HS050-12482 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr11:64682480-64684430 
Target genes
Number: 45             
NameEnsembl ID
BADENSG00000002330
TRMT112ENSG00000173113
PRDX5ENSG00000126432
AP003774.5ENSG00000231492
SLC22A11ENSG00000168065
NRXN2ENSG00000110076
RASGRP2ENSG00000068831
PYGMENSG00000068976
SF1ENSG00000168066
MAP4K2ENSG00000168067
MEN1ENSG00000133895
AP001187.11ENSG00000230835
EHD1ENSG00000110047
AP001187.1ENSG00000203400
MIR192ENSG00000207648
MIR194ENSG00000207596
AP001187.9ENSG00000229719
ATG2AENSG00000110046
PPP2R5BENSG00000068971
GPHA2ENSG00000149735
C11orf85ENSG00000168070
BATF2ENSG00000168062
ARL2ENSG00000213465
SNX15ENSG00000110025
SAC3D1ENSG00000168061
CDCA5ENSG00000146670
ZFPL1ENSG00000162300
C11orf2ENSG00000149823
AP003068.6ENSG00000187066
AP003068.9ENSG00000254501
AP003068.12ENSG00000255173
MRPL49ENSG00000149792
FAUENSG00000149806
SYVN1ENSG00000162298
HIGD1AP10ENSG00000254455
U2ENSG00000222477
AP003068.17ENSG00000255058
SPDYCENSG00000204710
PGAM1P8ENSG00000249251
AP003068.18ENSG00000255200
CAPN1ENSG00000014216
AP003068.23ENSG00000254614
SLC22A20ENSG00000197847
POLA2ENSG00000014138
CDC42EP2ENSG00000149798
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
GTTGCAGGCA CAGGACAACA TGGGCACATG TATGGCAGAG TCCAGAATAC CCATGTTCAC 60
CCTGGATGAG CAGAGTTCAA AGGGACAGTG TCCAAGAGAG GGGCTGACCT AATGCCAGAT 120
GGGACCCCCC CCCCCCACCA CCAACCCCAA ACACCTAGTG TAGCTGTGCC TCTCTGTGAG 180
GCACAAGGCT GAGCCCCTGG CTAAAATGTC CATGCTGGAG TTGTACCCCT GCCAACCTGG 240
AAGCTCCTGG AGGGCTGTAC CCCACCTGCC TCCCCCGTCA CCCCAGGTGC CACCCAGAAA 300
GGGCCTCAGT AAACTGGTTG GATCCAAGAA TAAAAAAGCA CATGGCAGAG CAGATGGGAG 360
TCCAAATTCC TCACCCAGAG ACCCACAGCT CGGGAAACTG AGGCCTAGAG ACAGGACTAA 420
TCTAGTCACC CAGTATACAA CAGGGACTGA GACTGGGATG CGGGCCTCTT TCTTTTCATG 480
CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG 540
CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG CCTGCATTCC ACCAGGGCCC 600
TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG 660
GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG TGGTTCATGC CTATAATCTC 720
AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA 780
CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG 840
GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC CAGAATTCAC AGACAGCAGG 900
CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC TACCCCACAT TTGCTCACCA 960
GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA 1020
GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT GCTGCTCTGG ACCTGGTGGA 1080
TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG 1140
TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG ACCTTACACC TCTTGGCCTC 1200
CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA TCTCCCCACC TTTCCTCCAG 1260
GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG TGGGAGATGT AGGTGGGGGC 1320
CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC TCTCCCAAAA GCAGGAAGTA 1380
GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT ACTGACGTAC TGACGCGGTT 1440
GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG GGCTCAGGAC CGTGGGGTCA 1500
AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG CTCCGGACCC CTACCAGCTT 1560
CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG GCCCAGCTCA GTTCCTACGC 1620
TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT TAACTCAGCC CCCAAACTCG 1680
ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC TCTCCAGCCT CAGTTTCTCC 1740
TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG AACTGAAGAG 1800
GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT CCCCTGGCCT CTCTACGCCC 1860
GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT CAGGTCGCTG CGCTCCCACC 1920
CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1950