EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS136-17836 
Organism
Homo sapiens 
Tissue/cell
Monocyte 
Coordinate
chr7:13889290-13890760 
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
AAACAGCAAC AGTGAAAGAA AAGAAAAAGA GAAAGAAAGA AAGGAAGGAA GGAAGGAAGG 60
AAGGAAGGAA GGAAGGAAGG AAGGAAGGAA AAGGAAAAGG AAAGAAAGGA AAGAAGGAAG 120
GAAGGAAAGA AAAAAAGAAA GAAAGAGAAA AATGCCTGAG ATAATTAGAG AATACAGAGC 180
ACAAGCCTGA TCTTCAAATA TTGTCTAAAG TCCACTAACG AAATATTAGC TGTATTGTTT 240
AAGCCAATGT GAGGTGTATT TTTGTGGTGC TTGTGGTGGT GGTTGTTGTT TGGTTGTGGA 300
GTTTTCTTGC ATTTCGACTG GAAAAAGATC CTGATACATA AGCAGAGATG CAGAAAAATA 360
AATCTATAAT TATAAAATCC GTATGGTGGG GTTCTTCTGC CGGGCCCATT AGAACACGGT 420
ATGTTATTTC ACACACTCTC TTATTGAAGT AAAATTACCC TTCAGCCCCT AACCATGCTC 480
GGCAGGAGAG ACTGTGCTGG GAAGACCACT GTTTCTAATG TATGTTACAA AGTTGATGCT 540
AACAAGCATT TTAAACAAGT TAAGTGCATC ACTGCTGTTT CGCCTTCTCG TGGTTAGAGG 600
TGTGAGTCAT GCTTCCTGTT AAGCCCAGAG ACAGTGCCTG TTTGAGGTTT GATTATTTGG 660
TAACAAAATG GAAAGCACAC TGCTGCTGTG TCAGTGAGCT GGAAGCAATC AACATTTACT 720
AGGCTTACAC ACATGAGAAA TGCAAATAGG TTTCATTTGC TGGGATATGG GTTGGTGGCT 780
TGACTCAAAC ATTTCATACC CCCAGGAAAA AGGAAGTTAA ACCACAGGAT TAATCCTTGA 840
CTAAATCTTG AGGCATTTTT AACCACAAAT TAGAAAATTA AAACCAAAAT GTATTCTGCC 900
ATTCCAAAAC CAAAGAGCTA AGCTCTTACT TCAGAGGTTG GCAAACTCCA CCATGTTGGC 960
CCATTTCACT TGACTCTTAC CTACCTACTG GTTTACTTTT ACTGGCTTTC TGCCAGCCTC 1020
TCCAAGGCAG AGCCATGAAA CCATGACTCC CAGCTGTGGA ATCAGAGACT GGGTGGCAAT 1080
TAGGCTTCAG AGGGCACCAG GAGCTTCCAG TGATACGTAA TTGCTGAATT TCTGGGGATA 1140
ATTACAGGGG GTCTTTGGGC TGTCTGGGGA AAAAAAAAAT CAATCTGAAA ACTCACAACG 1200
TATACGGTTA CTGTATTACT GTAAGAATCA TAACTTACAA AGTTAAAGAT AGTTGTATTC 1260
CAACGGCATG ATAATGCAGA AATGGTAAAG AAGAGGTAGC ATCCATGCCA TTCAAGATAT 1320
AAAGTTCTCA GTTAATAGTA GTTGATAGCG ATGATGCTTT TACTTTAAGA AAGCAAGAGA 1380
AGTAATAGTT CCTTGAACTC ATCTTATAAA CGCCTGATTT TATTCCACAG AGATCTTACC 1440
AGGAGAGTCA GAATCTTTTA AGGAAACTGC 1470