EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-10460 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr12:111836220-111838020 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs149212747chr12111836772hg19
TF binding sites/motifs
Number: 33             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr12:111837758-111837776GGAAGGAAGGAAGGAAAG+10.53
EWSR1-FLI1MA0149.1chr12:111837734-111837752GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr12:111837738-111837756GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr12:111837742-111837760GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr12:111837746-111837764GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr12:111837750-111837768GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr12:111837754-111837772GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr12:111837706-111837724GAAAGAAGGAAAGGAAGG+6.18
EWSR1-FLI1MA0149.1chr12:111837762-111837780GGAAGGAAGGAAAGGAAG+6.98
EWSR1-FLI1MA0149.1chr12:111837710-111837728GAAGGAAAGGAAGGAAGG+7.26
EWSR1-FLI1MA0149.1chr12:111837767-111837785GAAGGAAAGGAAGGAAGG+7.26
EWSR1-FLI1MA0149.1chr12:111837775-111837793GGAAGGAAGGAAGGAGTC+7.63
EWSR1-FLI1MA0149.1chr12:111837714-111837732GAAAGGAAGGAAGGAAGA+8.73
EWSR1-FLI1MA0149.1chr12:111837718-111837736GGAAGGAAGGAAGAAAGG+9.25
EWSR1-FLI1MA0149.1chr12:111837722-111837740GGAAGGAAGAAAGGAAGG+9.25
EWSR1-FLI1MA0149.1chr12:111837730-111837748GAAAGGAAGGAAGGAAGG+9.6
EWSR1-FLI1MA0149.1chr12:111837771-111837789GAAAGGAAGGAAGGAAGG+9.6
EWSR1-FLI1MA0149.1chr12:111837726-111837744GGAAGAAAGGAAGGAAGG+9.72
Foxd3MA0041.1chr12:111837115-111837127AAACAAACAAAC-6.32
HNF1AMA0046.2chr12:111836796-111836811TGTTAATTATTGATT-6.74
HNF1BMA0153.2chr12:111836797-111836810GTTAATTATTGAT+6.28
JUN(var.2)MA0489.1chr12:111837433-111837447TAGAAATGACTCAT+6.43
ZNF263MA0528.1chr12:111837707-111837728AAAGAAGGAAAGGAAGGAAGG+6.09
ZNF263MA0528.1chr12:111837731-111837752AAAGGAAGGAAGGAAGGAAGG+6.16
ZNF263MA0528.1chr12:111837763-111837784GAAGGAAGGAAAGGAAGGAAG+6.23
ZNF263MA0528.1chr12:111837755-111837776GAAGGAAGGAAGGAAGGAAAG+6.48
ZNF263MA0528.1chr12:111837719-111837740GAAGGAAGGAAGAAAGGAAGG+6.54
ZNF263MA0528.1chr12:111837735-111837756GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr12:111837739-111837760GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr12:111837743-111837764GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr12:111837747-111837768GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr12:111837751-111837772GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr12:111837723-111837744GAAGGAAGAAAGGAAGGAAGG+7.16
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_00313chr12:111834286-111837931Adipose_Nuclei
SE_09337chr12:111834152-111838375CD14
SE_32074chr12:111836085-111836790Gastric
SE_38040chr12:111833977-111838428HUVEC
SE_40792chr12:111836333-111837557Left_Ventricle
SE_42263chr12:111836045-111837570Lung
SE_48851chr12:111836174-111837533Right_Atrium
SE_52677chr12:111836083-111837384Small_Intestine
SE_53326chr12:111836118-111837582Spleen
SE_56066chr12:111836089-111838187u87
SE_62745chr12:111834432-111886877Tonsil
SE_67523chr12:111836089-111838187u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12111836487111836654
chr12111836884111837500
Number: 1             
IDChromosomeStartEnd
GH12I111396chr12111834288111838135
Enhancer Sequence
AGTAAGTGAT TAAGAGGTAG GGCACTACAG TGAGGCCAGT CTTTAGTCCA CACCAGCTGC 60
TTCATTGCCA GTCGTGTGAC ATGGACATGT CACTTCACTG CCCTGTGCCT CAGTTCCTTC 120
ATCTGACAAA TGGGAAAATG AATAGCAAAC CGTTCATTTG GGGTGGAAGA GATAAGGCCT 180
GTGATGTTCT CAGTGTGGCG CACGCTTCCA TAAATGGAGT CCAGATTGTA AATACTGTTC 240
ATGCTTTTCT TAGGGAAGGA CTTGTGGCAA TTTTAGCTTC TAAGGCACTG GGAGGACAGA 300
AAACAGAACT GAATCCAAGG GAAGGAAGCA CAGGGAGAGA TGACATCAGG CACTTGAGCT 360
CAGCAGATCA GACCCTGAGC CCAGGAATCG GCCTTGGGAG TTCTGCCCAC CCAGGCAAAA 420
AGGGAAGAAC CCAGTAATGT AATTATTTTC TGGCCTGGGG CAGATGTGTA TTGACCAAGG 480
GGGACCATTT CCTGAGCCCT CTTGGTCTCT GTTGGACCCT AATGGGTGGG AAAAGGGTTG 540
GTTGGACCTC ACCCCCCCAA GGTTTCTTGA GCTCTGTGTT AATTATTGAT TGCTGGGTAA 600
CAAATTACTC CTGCATTTAC TGGCTTAAAA CAGCAAACCT TTATTATCTC ATATGGTTTT 660
AGGAATTCAC ATGCAATCTG ACTTAGCTTG TAGTTCAGGG TCTCTCACTC CTGAGATGGT 720
AGTCCGAAAC ATGGGCTGGT GGCACGCACA TGCAGTTGCA GCTATTTGAG AGGCCGAGAC 780
AGGAGGATTG TTTGAGCCTA GAAGTTCAAG GCTATAGATC GTGCTATATG ATCGTGCCTG 840
TGAATAGCCA TTGCATTCCA GTCTGGGCAA TGAAACAAGA CCCCGTCTTT TAAATAAACA 900
AACAAACAAA AATGGGTTAG GACTGTTCTC ATCTGGGGTC CAACTGGGGC TGGATGATTC 960
ACTTCCAGGA TAGTTGGAAG TGATGGTTTC AGTCCTGGCT GTTGCCAGGA GGTCTCTGTT 1020
CCTTGCTGGC TGGTGGCAGG AAGCCTCAGT TCCTCTTCAC ACGGACCTCC ATAAAGCTAC 1080
TTGGGTGTCC TTAAGACACG GTGGCTGGCT TCTCCCAGAG TGGATGGCTC AAGAGAGTAC 1140
AAGGAGAAGC CTAAATGCTT CTTATGACTC AGTCTCAGAA GTCACACAGC GTCACTTCCA 1200
CTTTAGTCTC TGTTAGAAAT GACTCATTAA GGCCAGGTGT GGGGGCTCAC GCCTGTAATC 1260
CCAGCACTTT GGGAGGCCGA GGCGAGCGGA TCACGAGGTC AGGAGATCAA GACCATCCTG 1320
GCTAACACAG TGAAACCCTG TTTCTACTAA AAATACAAAA AATTAGCTGG GCGTGGTGGC 1380
TCGTGCCTAT AGTCCCAGCT ACTCAGGAGG CGGAGGTTGC AGTGAGCCGA GATCGCACCA 1440
CTGCAGTCCA GCCTGGGTGA CAGAGCAAGA CTCTGTCAGA AAGAAAGAAA GAAGGAAAGG 1500
AAGGAAGGAA GAAAGGAAGG AAGGAAGGAA GGAAGGAAGG AAGGAAGGAA GGAAAGGAAG 1560
GAAGGAAGGA GTCATTAAGT CCAGCCCACA CTCAAGGGCA GGGGAATCAG GTTCCACCTT 1620
TTCAAGGGAG GTATGTCAAA GAAGTGTGGA CTGTTTTTAA GCCACGAGGA GCACCTGTTA 1680
TGTGCCAAGA ACTGTGCTCA CAAGAGTGAG CAAGACACAC AAATGCCTGG CCGAGTGGAG 1740
CTGACCTGCT CCTGGGGGTG GGGGAAAGAG ACTGCCAATA AACAGATGAA TCAATGATTC 1800