EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS023-22798 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr7:13888700-13890820 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56805921chr713888699hg19
TF binding sites/motifs
Number: 31             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr7:13889332-13889350GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr7:13889336-13889354GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr7:13889340-13889358GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr7:13889344-13889362GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr7:13889348-13889366GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr7:13889352-13889370GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr7:13889356-13889374GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr7:13889360-13889378GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr7:13889389-13889407GAAAGAAAGGAAAGAAGG+6.98
EWSR1-FLI1MA0149.1chr7:13889320-13889338GAAAGAAAGAAAGGAAGG+7.02
EWSR1-FLI1MA0149.1chr7:13889405-13889423GGAAGGAAGGAAAGAAAA+7.52
EWSR1-FLI1MA0149.1chr7:13889393-13889411GAAAGGAAAGAAGGAAGG+7.97
EWSR1-FLI1MA0149.1chr7:13889401-13889419AGAAGGAAGGAAGGAAAG+8.46
EWSR1-FLI1MA0149.1chr7:13889324-13889342GAAAGAAAGGAAGGAAGG+8.57
EWSR1-FLI1MA0149.1chr7:13889364-13889382GGAAGGAAGGAAGGAAAA+9.07
EWSR1-FLI1MA0149.1chr7:13889397-13889415GGAAAGAAGGAAGGAAGG+9.47
EWSR1-FLI1MA0149.1chr7:13889328-13889346GAAAGGAAGGAAGGAAGG+9.6
IRF1MA0050.2chr7:13889415-13889436AAAGAAAAAAAGAAAGAAAGA-6.34
IRF1MA0050.2chr7:13889309-13889330AAAGAAAAAGAGAAAGAAAGA-7
RREB1MA0073.1chr7:13889566-13889586TGGTGGTTGTTGTTTGGTTG-6.33
ZNF263MA0528.1chr7:13889373-13889394GAAGGAAAAGGAAAAGGAAAG+6.02
ZNF263MA0528.1chr7:13889402-13889423GAAGGAAGGAAGGAAAGAAAA+6.11
ZNF263MA0528.1chr7:13889329-13889350AAAGGAAGGAAGGAAGGAAGG+6.16
ZNF263MA0528.1chr7:13889361-13889382GAAGGAAGGAAGGAAGGAAAA+6.56
ZNF263MA0528.1chr7:13889333-13889354GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr7:13889337-13889358GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr7:13889341-13889362GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr7:13889345-13889366GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr7:13889349-13889370GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr7:13889353-13889374GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr7:13889357-13889378GAAGGAAGGAAGGAAGGAAGG+6.94
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr71388948213890570
Number: 1             
IDChromosomeStartEnd
GH07I013848chr71388812913890773
Enhancer Sequence
CACACACACA CACACACACA CACACACACA CAGCTAAAGC CCAGGAGTAG TTCTGTAGGA 60
AATATCCACT GTAAAAGGAA AATGGACGTA CAACTGAGGA ATCAGATTAG GAGATTTGGC 120
AAAATCACAA AGATAATTTT GCTAACATTG GAGTCACCAA CATAAAGCTC CACAATTTAG 180
GCCAATACTG GGTTGCACAG TATAGTGACA TTGTGGCTTT CCTCCCTGGA ATCACCATGT 240
CACTGCCATG CTGTTGTGTC CTGGATTTAG CTGACTTTGG CAGGACAAGC CCTCTCTTAT 300
CTCTGGGGGG TGATGGGAGA GGGCTAAGCG GCCTCATCCA GTAAACTGCC TTTGCTTTCA 360
CAGGTTCAGG ATGGTCAGGG GTACAGGCCT AAGCCCTACA TTGTCCACAG TGATTAGTAG 420
TTAGTTCAGA GGCAGGGATG TGAATGACCT AATTTTGTCT AATCAGTAAA GCCTAATACT 480
TTTATTCAGT AGTTGAATAA AGATAAAAAG CTCTATTATT CCAGATCTTG TGGTTAGAGA 540
TAGGAACCCT GACACCACTG CGGCCATTTT CTTACTATGA CAAAACAAGC AAACAGCAAC 600
AGTGAAAGAA AAGAAAAAGA GAAAGAAAGA AAGGAAGGAA GGAAGGAAGG AAGGAAGGAA 660
GGAAGGAAGG AAGGAAGGAA AAGGAAAAGG AAAGAAAGGA AAGAAGGAAG GAAGGAAAGA 720
AAAAAAGAAA GAAAGAGAAA AATGCCTGAG ATAATTAGAG AATACAGAGC ACAAGCCTGA 780
TCTTCAAATA TTGTCTAAAG TCCACTAACG AAATATTAGC TGTATTGTTT AAGCCAATGT 840
GAGGTGTATT TTTGTGGTGC TTGTGGTGGT GGTTGTTGTT TGGTTGTGGA GTTTTCTTGC 900
ATTTCGACTG GAAAAAGATC CTGATACATA AGCAGAGATG CAGAAAAATA AATCTATAAT 960
TATAAAATCC GTATGGTGGG GTTCTTCTGC CGGGCCCATT AGAACACGGT ATGTTATTTC 1020
ACACACTCTC TTATTGAAGT AAAATTACCC TTCAGCCCCT AACCATGCTC GGCAGGAGAG 1080
ACTGTGCTGG GAAGACCACT GTTTCTAATG TATGTTACAA AGTTGATGCT AACAAGCATT 1140
TTAAACAAGT TAAGTGCATC ACTGCTGTTT CGCCTTCTCG TGGTTAGAGG TGTGAGTCAT 1200
GCTTCCTGTT AAGCCCAGAG ACAGTGCCTG TTTGAGGTTT GATTATTTGG TAACAAAATG 1260
GAAAGCACAC TGCTGCTGTG TCAGTGAGCT GGAAGCAATC AACATTTACT AGGCTTACAC 1320
ACATGAGAAA TGCAAATAGG TTTCATTTGC TGGGATATGG GTTGGTGGCT TGACTCAAAC 1380
ATTTCATACC CCCAGGAAAA AGGAAGTTAA ACCACAGGAT TAATCCTTGA CTAAATCTTG 1440
AGGCATTTTT AACCACAAAT TAGAAAATTA AAACCAAAAT GTATTCTGCC ATTCCAAAAC 1500
CAAAGAGCTA AGCTCTTACT TCAGAGGTTG GCAAACTCCA CCATGTTGGC CCATTTCACT 1560
TGACTCTTAC CTACCTACTG GTTTACTTTT ACTGGCTTTC TGCCAGCCTC TCCAAGGCAG 1620
AGCCATGAAA CCATGACTCC CAGCTGTGGA ATCAGAGACT GGGTGGCAAT TAGGCTTCAG 1680
AGGGCACCAG GAGCTTCCAG TGATACGTAA TTGCTGAATT TCTGGGGATA ATTACAGGGG 1740
GTCTTTGGGC TGTCTGGGGA AAAAAAAAAT CAATCTGAAA ACTCACAACG TATACGGTTA 1800
CTGTATTACT GTAAGAATCA TAACTTACAA AGTTAAAGAT AGTTGTATTC CAACGGCATG 1860
ATAATGCAGA AATGGTAAAG AAGAGGTAGC ATCCATGCCA TTCAAGATAT AAAGTTCTCA 1920
GTTAATAGTA GTTGATAGCG ATGATGCTTT TACTTTAAGA AAGCAAGAGA AGTAATAGTT 1980
CCTTGAACTC ATCTTATAAA CGCCTGATTT TATTCCACAG AGATCTTACC AGGAGAGTCA 2040
GAATCTTTTA AGGAAACTGC AGCTATCTGT GAGCATTATT AAGTTGAAAT TCTTAATATA 2100
AAAAAAAAAT CCAGACACCA 2120