EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-04188 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr14:76013800-76016330 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 29             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr14:76016308-76016326CCTTCCCTCCCTCCCTTC-6.02
EWSR1-FLI1MA0149.1chr14:76016289-76016307CTTCCCTTCCTCCCTCCC-6.25
EWSR1-FLI1MA0149.1chr14:76016265-76016283TCTTCCTCCCTCCCTCCC-6.36
EWSR1-FLI1MA0149.1chr14:76016309-76016327CTTCCCTCCCTCCCTTCC-6.36
EWSR1-FLI1MA0149.1chr14:76016296-76016314TCCTCCCTCCCTCCTTCC-6.3
EWSR1-FLI1MA0149.1chr14:76016300-76016318CCCTCCCTCCTTCCCTCC-6.84
EWSR1-FLI1MA0149.1chr14:76016261-76016279CCTTTCTTCCTCCCTCCC-6.85
EWSR1-FLI1MA0149.1chr14:76016272-76016290CCCTCCCTCCCTCCTTCC-7.12
EWSR1-FLI1MA0149.1chr14:76016280-76016298CCCTCCTTCCTTCCCTTC-7.26
EWSR1-FLI1MA0149.1chr14:76016284-76016302CCTTCCTTCCCTTCCTCC-7.36
EWSR1-FLI1MA0149.1chr14:76016304-76016322CCCTCCTTCCCTCCCTCC-7.36
EWSR1-FLI1MA0149.1chr14:76016276-76016294CCCTCCCTCCTTCCTTCC-7.97
FOSL1MA0477.1chr14:76013877-76013888CATGAGTCACC-6.62
JUNDMA0491.1chr14:76013877-76013888CATGAGTCACC-6.02
ZNF263MA0528.1chr14:76016280-76016301CCCTCCTTCCTTCCCTTCCTC-6.24
ZNF263MA0528.1chr14:76016260-76016281CCCTTTCTTCCTCCCTCCCTC-6.3
ZNF263MA0528.1chr14:76016309-76016330CTTCCCTCCCTCCCTTCCTTC-6.88
ZNF263MA0528.1chr14:76016264-76016285TTCTTCCTCCCTCCCTCCCTC-6.8
ZNF263MA0528.1chr14:76016296-76016317TCCTCCCTCCCTCCTTCCCTC-6.91
ZNF263MA0528.1chr14:76016288-76016309CCTTCCCTTCCTCCCTCCCTC-7.19
ZNF263MA0528.1chr14:76016253-76016274TTCCCTTCCCTTTCTTCCTCC-7.27
ZNF263MA0528.1chr14:76016300-76016321CCCTCCCTCCTTCCCTCCCTC-7.29
ZNF263MA0528.1chr14:76016281-76016302CCTCCTTCCTTCCCTTCCTCC-7.32
ZNF263MA0528.1chr14:76016304-76016325CCCTCCTTCCCTCCCTCCCTT-7.34
ZNF263MA0528.1chr14:76016256-76016277CCTTCCCTTTCTTCCTCCCTC-7.4
ZNF263MA0528.1chr14:76016272-76016293CCCTCCCTCCCTCCTTCCTTC-7.6
ZNF263MA0528.1chr14:76016292-76016313CCCTTCCTCCCTCCCTCCTTC-8.03
ZNF263MA0528.1chr14:76016284-76016305CCTTCCTTCCCTTCCTCCCTC-8.21
ZNF263MA0528.1chr14:76016268-76016289TCCTCCCTCCCTCCCTCCTTC-9.07
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_18424chr14:76014446-76016504CD4p_CD25-_Il17-_PMAstim_Th
SE_19234chr14:76015394-76016544CD4p_CD25-_Il17p_PMAstim_Th17
SE_22816chr14:76014657-76016265CD8_primiary
SE_58818chr14:75935315-76038396Ly3
SE_61163chr14:75946267-76027852HBL1
SE_62931chr14:75980144-76016207Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr147601418076014465
chr147601550676015808
chr147601500376015159
chr147601595876016012
Number: 3             
IDChromosomeStartEnd
GH14I075547chr147601418076014465
GH14I075548chr147601502176015170
GH14I075549chr147601550676015808
Enhancer Sequence
TGTTGGTCAG GCTGGTCTCG AACTCCTGGC CTGAAGTGAT CCACCCGCCT GGGCCTCCAA 60
AGTGCTGGGA TTACAGGCAT GAGTCACCAT GCCCAGCCTA GGTGTCTTCT GGATTGCCCT 120
CCCATGCTCC CCTCACGGTG ACCTCCCACC TTCCATTCTT CACTGCTTTC TAGACCATGA 180
GCAGGTTGTC CCCTAGTCCG GGAGAAGGCC CAGTGCAGGA TGGCCTCACC TGGTGAGGTG 240
GTAAGTCAGG TTGACCTTCT CGTCTCCCAC TCATGACTCC ACTCACCCAG CCAACTGGCT 300
CCATCCTGAC AGCCAAGTCT CCGGATGCTG CAACCAGGCC CTGTGCCAGG CTGCCCTTCA 360
CATGGAAGGC GGTGTCTTCC TAATGCTCTC AAGGGGCAAC ATGCAGCTTG GGTCCACAGG 420
GACTTCTCTG CCAGTGGTGT ACATGTCCTG CTGAAGACTC CACCTCCCTT AGAAGGCGGT 480
GATACAGAGC ACAGGACTTG TCCTGTCCCC GCAGGGCTCC GCAGGCTGCC ATTTGAGCAC 540
TTTGAGGGCT CAGGGAACAC AGGGTCATCT TCAGTTTGGC AGAGCCTGAA ACCAGCATGC 600
TCCACCCCCC TGCTCTTCAG AGATCCCCAG GCCAAGTGCC TGCTGGCCTG CCTGACACAG 660
CCTTACCCAC ACCACTGCCC ACGAGCAAAG CCTGCAGCAG GGCCTGGCCA CACACAACCC 720
CTGCTGAGCC AGCTGGAGAC AAAAGCAACG GAGATCATTG TGCCAGGCGC CCACCTGATT 780
GAGCTCCTTC AGTAGCCACC CTCAGTCTCA TCCATTTGTC CTTTAGAGGG ACAGCCTCTG 840
CCTGCTGCCT CCCCGGTGGC ATCCCTCATG GGGTGACAGA AGGGAGGAGA AGTCCTGCTT 900
CCCTGTGTCA GTGCCCCCTG AACCCGCTGG CCAACCACTC TGGCCGGTTT GAGGCCAAGT 960
TTCAACTCTA GACCTCCCCT GTGTGTGTCT CTCCTGCCCC TCTCAGATGA TGCCAGTGTT 1020
GGGCTATTGT GATTATTAAA TGCCATAGAA GTTTGGATGA GCTGCATCCC AGCAGGTGGT 1080
GGGGTCACAG CCCCTTGGGA GGAGTCCAAC CCAACAGCCT CTGATGGCAC ATTGCAATCT 1140
TTGGGGCTCT CACCAGAGAA GCTGGTGCCC ATGGGAGCCT AGGATGTGGA CACTGGGCTG 1200
AGCCCCGTAA TTCAGAGCCT GGGAAGACAG CCCAGAAGAC GTTCCCTGAG TGCTGGCATT 1260
TCTCCCAGCA CAGAATCTTG CATTGTAACC TTTGGTCTCC CAACGAAACG TGGCAAAACA 1320
GGCTCCCCTT TCAGTGCAGA GCCTCCATGT GGACTGGGCA GATGTGTCAT GAGGAGGAGC 1380
TTTCTTAATT TCCTTCAGAA CCTGGATTTT GGTAGCTAAC GCTCTGTCTA GCTCTTTCCC 1440
ACCCCTCTGT TAACGAGAAG AGCAAAGAAG CCGATCTTCA CTTCAGATGT TGCAGTCATA 1500
AAATATAATT CATTTTTCTT TCATAATTAT TATTTTTTCT TTTTTTGAGA CACGGTCTCA 1560
CTCTGTCACC CAGGCTGGAG TGCAGTGGTG CAATCATGGC TCACTGCAGC CTTGACTACC 1620
CACACTCAAG CGATCCTCCC ACCTCAGCTT CCCAAGGTGT TGGGATTACA GGCATGAGCC 1680
ATTGCACCTG GCCTTCTTTC ACGATCTAAA GACGTAGAAC TTTGAGTCCA GCTTTCTTTG 1740
CTACTATCTC TGCCAGGGCC TGGCCTCTTG TGGGCAGGCT TTCTTTGAAT CAGAGATTTT 1800
CATCTCCACC CATGCTCTAG CACTGTGATT TTCCCCAGAA ACCCCCACAG AAGGCACATG 1860
ACTTCTGCCG GCATCTTCTG AATGACATTC AGGGCCAGAA CTAGAAAAGC AGAGTTCACG 1920
TGCACGGTTC CCATCTCTCA GCAAGGACTT CTCTTCCCCT TTCATTCTCT ACTTTCTACT 1980
GACCCCAGGC AGTTCCACTT CTCCTGTCTA GTCAGCCCGG TAGAGGTAGC AGGTAGCTGA 2040
GCCTGGAGCT GGTGCCAAGG CTGACTTCAT GTCCATGCAG GCAAATTGGA GAGGCAGCCA 2100
TGAATAGAAA TTTGAACATC CGTAGCTTTA ACCTTGGATG TTTCACCAAC CAGGTTCTGT 2160
CCCAGCCTTC TACCCATGAC AGGGATGGCT CCCTCAGTCT GGTGGGCCAC TTGACCCACA 2220
CTCAAACGCC TTCTACCCAG GCAGGCACTG TGAAAGCATG GGACCCACTG GATGTAGGGC 2280
AATTGGGAGT GGTGGAGAAT GTGGCAAACT AAGGAGAGTG TGCAGCTGTC TGTCGTTCAG 2340
TTCTCTCCCA TGGTGCCATG TGGGAATTTA GGCCTGGGCT TGCCATGTCT TCCAGTTTGT 2400
CAAGAAAAGC CAAAATCAGA ATTTCTACAT GAAATCTCTC AATTCTTTTT TTCTTCCCTT 2460
CCCTTTCTTC CTCCCTCCCT CCCTCCTTCC TTCCCTTCCT CCCTCCCTCC TTCCCTCCCT 2520
CCCTTCCTTC 2530