EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS154-19858 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr7:13888070-13890780 
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: 2             
ChromosomeStartEnd
chr71388816713889077
chr71388948213890570
Number: 1             
IDChromosomeStartEnd
GH07I013848chr71388812913890773
Enhancer Sequence
TCACTACTGA CAACCTCTAT CAACTCCTTC TTCTAAAATG AGACTTGTGA CTTGTGTTTT 60
TAATTTTTTA ACTGTTAGAT AATTATATCA TTCCTTTAAA ATATAGTAAG CTCCTTGATG 120
ACACACTCAA TCTCTCCCTT CTCCCAGAGT GCTTAATCAA TATTTGTTTC TTGAATTGAA 180
TAGAACTGAG TGGTAAGATT TCCCTCCAAT TTTGGTTATT TTCTAATATG AGAGTCTGGA 240
TGATCTACTC CCTCACGTAC ACAGTGCATG TGCCCTGGCG TGACTCGGCA GGCTCTGATC 300
ACCAGCCAAT TTTCGGCAGC AAACCCGTAT TTTTTTTTTA TTCTGAGAAA TTATAAAAAT 360
AACATTCCTG CCATCACTTC ATCAATTCAT AAAGTGACTT TAGTCTCTTG CTTTCTAATT 420
CCTTTCATTT CTCCTTTATA AGCCTGCCAA TAGCCTGGGC CTTTGCTGGC CTTACATATT 480
TAATCAGAGT AACCAATGCT GAGGATTTTT ACAGGGAATT AAGTTTGATT TGTTTTGAAA 540
CATTTATTTA TTCCATATGG CATTTAAGTG ACTGAATTAT TTTTGGTGTT GGAATGAGGT 600
TGCATAAACT GGATTCAAAT TTAAAACAGA CACACACACA CACACACACA CACACACACA 660
CAGCTAAAGC CCAGGAGTAG TTCTGTAGGA AATATCCACT GTAAAAGGAA AATGGACGTA 720
CAACTGAGGA ATCAGATTAG GAGATTTGGC AAAATCACAA AGATAATTTT GCTAACATTG 780
GAGTCACCAA CATAAAGCTC CACAATTTAG GCCAATACTG GGTTGCACAG TATAGTGACA 840
TTGTGGCTTT CCTCCCTGGA ATCACCATGT CACTGCCATG CTGTTGTGTC CTGGATTTAG 900
CTGACTTTGG CAGGACAAGC CCTCTCTTAT CTCTGGGGGG TGATGGGAGA GGGCTAAGCG 960
GCCTCATCCA GTAAACTGCC TTTGCTTTCA CAGGTTCAGG ATGGTCAGGG GTACAGGCCT 1020
AAGCCCTACA TTGTCCACAG TGATTAGTAG TTAGTTCAGA GGCAGGGATG TGAATGACCT 1080
AATTTTGTCT AATCAGTAAA GCCTAATACT TTTATTCAGT AGTTGAATAA AGATAAAAAG 1140
CTCTATTATT CCAGATCTTG TGGTTAGAGA TAGGAACCCT GACACCACTG CGGCCATTTT 1200
CTTACTATGA CAAAACAAGC AAACAGCAAC AGTGAAAGAA AAGAAAAAGA GAAAGAAAGA 1260
AAGGAAGGAA GGAAGGAAGG AAGGAAGGAA GGAAGGAAGG AAGGAAGGAA AAGGAAAAGG 1320
AAAGAAAGGA AAGAAGGAAG GAAGGAAAGA AAAAAAGAAA GAAAGAGAAA AATGCCTGAG 1380
ATAATTAGAG AATACAGAGC ACAAGCCTGA TCTTCAAATA TTGTCTAAAG TCCACTAACG 1440
AAATATTAGC TGTATTGTTT AAGCCAATGT GAGGTGTATT TTTGTGGTGC TTGTGGTGGT 1500
GGTTGTTGTT TGGTTGTGGA GTTTTCTTGC ATTTCGACTG GAAAAAGATC CTGATACATA 1560
AGCAGAGATG CAGAAAAATA AATCTATAAT TATAAAATCC GTATGGTGGG GTTCTTCTGC 1620
CGGGCCCATT AGAACACGGT ATGTTATTTC ACACACTCTC TTATTGAAGT AAAATTACCC 1680
TTCAGCCCCT AACCATGCTC GGCAGGAGAG ACTGTGCTGG GAAGACCACT GTTTCTAATG 1740
TATGTTACAA AGTTGATGCT AACAAGCATT TTAAACAAGT TAAGTGCATC ACTGCTGTTT 1800
CGCCTTCTCG TGGTTAGAGG TGTGAGTCAT GCTTCCTGTT AAGCCCAGAG ACAGTGCCTG 1860
TTTGAGGTTT GATTATTTGG TAACAAAATG GAAAGCACAC TGCTGCTGTG TCAGTGAGCT 1920
GGAAGCAATC AACATTTACT AGGCTTACAC ACATGAGAAA TGCAAATAGG TTTCATTTGC 1980
TGGGATATGG GTTGGTGGCT TGACTCAAAC ATTTCATACC CCCAGGAAAA AGGAAGTTAA 2040
ACCACAGGAT TAATCCTTGA CTAAATCTTG AGGCATTTTT AACCACAAAT TAGAAAATTA 2100
AAACCAAAAT GTATTCTGCC ATTCCAAAAC CAAAGAGCTA AGCTCTTACT TCAGAGGTTG 2160
GCAAACTCCA CCATGTTGGC CCATTTCACT TGACTCTTAC CTACCTACTG GTTTACTTTT 2220
ACTGGCTTTC TGCCAGCCTC TCCAAGGCAG AGCCATGAAA CCATGACTCC CAGCTGTGGA 2280
ATCAGAGACT GGGTGGCAAT TAGGCTTCAG AGGGCACCAG GAGCTTCCAG TGATACGTAA 2340
TTGCTGAATT TCTGGGGATA ATTACAGGGG GTCTTTGGGC TGTCTGGGGA AAAAAAAAAT 2400
CAATCTGAAA ACTCACAACG TATACGGTTA CTGTATTACT GTAAGAATCA TAACTTACAA 2460
AGTTAAAGAT AGTTGTATTC CAACGGCATG ATAATGCAGA AATGGTAAAG AAGAGGTAGC 2520
ATCCATGCCA TTCAAGATAT AAAGTTCTCA GTTAATAGTA GTTGATAGCG ATGATGCTTT 2580
TACTTTAAGA AAGCAAGAGA AGTAATAGTT CCTTGAACTC ATCTTATAAA CGCCTGATTT 2640
TATTCCACAG AGATCTTACC AGGAGAGTCA GAATCTTTTA AGGAAACTGC AGCTATCTGT 2700
GAGCATTATT 2710