EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-39632 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr8:99316600-99319420 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11785622chr899317739hg19
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr8:99319241-99319259TCTTCCTTCCTTCCTTCC-10.05
EWSR1-FLI1MA0149.1chr8:99319225-99319243CTTTCTCTCCTTCCTTTC-6.03
EWSR1-FLI1MA0149.1chr8:99319221-99319239CTTTCTTTCTCTCCTTCC-6.16
EWSR1-FLI1MA0149.1chr8:99319229-99319247CTCTCCTTCCTTTCTTCC-7.64
EWSR1-FLI1MA0149.1chr8:99319245-99319263CCTTCCTTCCTTCCTCTC-8.32
EWSR1-FLI1MA0149.1chr8:99319233-99319251CCTTCCTTTCTTCCTTCC-9.25
EWSR1-FLI1MA0149.1chr8:99319237-99319255CCTTTCTTCCTTCCTTCC-9.25
IRF2MA0051.1chr8:99318523-99318541GGAAAGCGAAACCCTCCA+6.48
IRF9MA0653.1chr8:99318521-99318536AAGGAAAGCGAAACC+6.28
RREB1MA0073.1chr8:99318795-99318815CCCCCAAACACACACACCGC+7.28
ZNF263MA0528.1chr8:99319298-99319319CTCTCTTTCTTCCTCTCCTCT-6.08
ZNF263MA0528.1chr8:99319260-99319281CTCTCATTCTCCTCTTCCCTC-6.12
ZNF263MA0528.1chr8:99319201-99319222TTTCCTTCTTTTTTCTCCTTC-6.13
ZNF263MA0528.1chr8:99319293-99319314TCTTTCTCTCTTTCTTCCTCT-6.23
ZNF263MA0528.1chr8:99319237-99319258CCTTTCTTCCTTCCTTCCTTC-6.28
ZNF263MA0528.1chr8:99319336-99319357CTCTCCCCTCTCCTCTCCTCT-6.32
ZNF263MA0528.1chr8:99319217-99319238CCTTCTTTCTTTCTCTCCTTC-6.43
ZNF263MA0528.1chr8:99317789-99317810CTCTCCTCATTCTCCTCCATC-6.54
ZNF263MA0528.1chr8:99319233-99319254CCTTCCTTTCTTCCTTCCTTC-6.54
ZNF263MA0528.1chr8:99317786-99317807CTTCTCTCCTCATTCTCCTCC-6.61
ZNF263MA0528.1chr8:99319241-99319262TCTTCCTTCCTTCCTTCCTCT-6.66
ZNF263MA0528.1chr8:99319270-99319291CCTCTTCCCTCCCCCTCCCTC-6.8
ZNF263MA0528.1chr8:99319229-99319250CTCTCCTTCCTTTCTTCCTTC-6.97
ZNF263MA0528.1chr8:99319331-99319352TTCCCCTCTCCCCTCTCCTCT-7.07
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr89931805599318682
chr89931868899318745
chr89931681599319207
Number: 2             
IDChromosomeStartEnd
GH08I098304chr89931712199317270
GH08I098305chr89931797799319148
Enhancer Sequence
AAAAATTCTT TTTCAGAGTC TCACTCTGTT TCCCAGGCTG GAGTGCAGTG GCAAAATCTT 60
GGCTCACTGC AACCTCCGCC TCCCAGATTC AAACGATTCT CATGCTTCAG CCTCCCAAGT 120
AGCTGGGATT ACAGGCACCA CCACACCCAG CTAATTTTTT TTTTTTTTTA ATTTTTAGTG 180
GAGATGGGGT TTTGCTATGT GCTATGTTGG CCAGGTTGGT CTTGAACTCC AGGCCTCAAG 240
TGATCCACCC GCCTTGGCCT CCCAAAATGC TTGGATTATA GGCATGAGCC ACCATGCCTG 300
GTGAAAATTT GCATTTTTAA AAAGCAAAAG CAAACACCTC AGCTTAGAGA AACTAAATTA 360
TTTACCTAAT GTTCACTGCT GGTTTGTGGT GGAGCCAAGA CTTCTGCTGC TCAATGAAGA 420
TGTCCAGGTA GAAGCGTATA CTAATCAGGG CTCTTCAGAG AAACAGAGCT AATAGGAGAT 480
AGGCATACAC ACATGCACAC GCACACAGAC TTATGATGAG GAATTGGCTC ACATGATTAT 540
GAAGGTGAAG TCCCAAGATC TATAGTTGGC AAACTGAACA CCCTAAAGAG CCAATGGTGC 600
AGTTTCAGTC TGAGTCTGAA GGCCTGAGAA CCAGGAGAGT CAGTGGGGTA GGTTCCAGCC 660
CAAAAGTGGG CAGGCCTGAG TCCCAAGAAG AGCTGATTTT TCAGTTAGAT TTCAAAGGCA 720
GGAAATGACC CATGTTCCAG CTCAAGCCAT CAGGCAGCAG GGGTTCCCTC TGACTCAGTC 780
TTTTTGTTCT ATTCAGGTCT TCAGTCAACT GATGAGACCC ACCCACATTA GGGAGCATAG 840
TCTGCTGTAC TCAGTCTACC AATTCAGCTA TGAAGCTCCT CCAGAAACTC CCGCACAGCC 900
ACATCCCAAA TAATGTTTGG CCAAATGTCT GGGTACCCTG TGGCCCGGTC AAGTGGACAC 960
ATGAAAGTCA CCATCACAGT GGGGTCCTCA AGGAAAGGAA TGAAAGAGAC AATCCAGCTT 1020
TGCATTTAGC ACTGATGCAA TGGCCTGTGA AACCAGACGT GACAAACGTG GCAAGTAGAA 1080
GTGTCACAGA CATAAATTTG AGCATTTCTC AGATTTTTCT TTGCCTGGAG TTTGATCTCA 1140
ATAGTCATTC AATTTGTCCC TTAGGACAAA TTTATTTTCT CTCTTTCTTC TCTCCTCATT 1200
CTCCTCCATC ACCATTATCA TCATCATTGT CACTGTCATA ATCAACATCC AAAGTGTATG 1260
GAGTGCCTGC ACTCACGTGG CTCTGTACCA AGAAGGAATT TGGAATTCAT GGAGGAAAAT 1320
GGATCTGTCC CTTGCTGTAA GTGGCTTAAT TCCAGTTTAA GAGACAGAAC ATACATAAAA 1380
AGATAAATAA GTATAAATCA ACTAGGAACT CGATAACTAA GTGCTAAATA CAGGAGGATA 1440
TGAATCTTGG ATTCCAAAAA AAGGAGTGAT TTTCGGGCTG GACAGGGTCT GGAAAAGCTT 1500
CAAGGAGGTC GAGGTTCTTG AGCAGGGCCT GAGAAAAGAG TGTGGCTGAC GCAAGTGTGA 1560
CAAGGAGAGA GTATGGCAGG AATATAGAAC ACCCAGAGGG AAGTGGGAAG TGCAAATGTG 1620
TGTGCAGGGA CAGCGAGTCA TGGCTGGGTG GGCACCCGTG CCATGGAACA GCTTGATGCC 1680
TGGAGAGCAA CTCCCAGAAA CAGCTTTTGG CCCAGATTGC TAATTAGAAT TTTTTACTGT 1740
GTGTGAAATT TCCAGGATCA GCATGGAGTG TCATCTGCGT CTCCTGCAGG CGTCTCCTCC 1800
CAAACACGGC TTCCTAAACC TGTCTTGCCA GTCAAGCCCC ACAGCTGCTC TGCCGAGTTA 1860
TACAGGCTTC CTCTAAAAAG CTGTTCTCCT GGACTTGCAT GTGCTTAAAG GGAAGAAAAG 1920
CAAGGAAAGC GAAACCCTCC ACTTGTTTCC AGGTTCTGAG CGAATCTTGT TTTTATACTA 1980
TTTGTCCTGT TATCTGGATC CACAGCACTG GTGTGTCTTA GACGATAAGG AAAGCAGGGA 2040
CTACTCCAGT AGTTCTCTCT GCAGGGCCCT GCTGTGTGCT GTGGCCTCTC TGGGTTCTTC 2100
ACGAGTGCCT TGGGGTTGTG ATGAAAACTA CATGTGTAAT GAGGCAGAGT AAGCTTTGCC 2160
TCCTGTCAAC CAATAGGGCA CCCCCTAGCA ATTCCCCCCC AAACACACAC ACCGCCCTGA 2220
AATTCCCCAA GGCCCTCATT TGGGTGCTCC TGGGGGCAGG GAGGGTTATG AAGAGAGGCA 2280
TACACTGTGC AAAGCAGCAC GTGCTCCAGG TCTGGTTCTG CCACCAACTA GCTGGGTGAC 2340
CTTGGGCAAG TTCCTGTATC TCCCTGGGCC TCATCTGTGA AATGAGAGGC TTGGACTATA 2400
TCATTCCAAA TGTTTCCAAC TCTGAAGTAT GAGTCTAGAA CTTTTATCTT CTTCACATTA 2460
TAGCAGATTT TTTTTTTTTT TAACCCCTGG CTACTTAGGG GAAGAGAGAA TGGCTCTAGA 2520
AGGTACTAAT CCGTCTTCCT ACAACATCTT GGGATATCTG GTAGTCGCTA GTCAAAGAGG 2580
GTTAGTTTTC CCCCCCCAAT TTTTCCTTCT TTTTTCTCCT TCTTTCTTTC TCTCCTTCCT 2640
TTCTTCCTTC CTTCCTTCCT CTCTCATTCT CCTCTTCCCT CCCCCTCCCT CTCTCTTTCT 2700
CTCTTTCTTC CTCTCCTCTG CGCTCTCCCT TTTCCCCTCT CCCCTCTCCT CTCCTCTCCT 2760
TTTATTTATT TATGTATTTA TTTATTTATT TATTATACTT TAAGTTTTAG GGTACATGTG 2820