EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-07235 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr11:34673350-34674800 
TF binding sites/motifs
Number: 20             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ALX3MA0634.1chr11:34673449-34673459TCTAATTAAA+6.02
EWSR1-FLI1MA0149.1chr11:34674686-34674704ACATCCTTCCATCCTTCC-6.93
EWSR1-FLI1MA0149.1chr11:34674690-34674708CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674698-34674716CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674706-34674724CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674714-34674732CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674722-34674740CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674694-34674712CCATCCTTCCATCCTTCC-7.93
EWSR1-FLI1MA0149.1chr11:34674702-34674720CCATCCTTCCATCCTTCC-7.93
EWSR1-FLI1MA0149.1chr11:34674710-34674728CCATCCTTCCATCCTTCC-7.93
EWSR1-FLI1MA0149.1chr11:34674718-34674736CCATCCTTCCATCCTTCC-7.93
EWSR1-FLI1MA0149.1chr11:34674726-34674744CCATCCTTCCATCCTTCC-7.93
NFE2L1MA0089.2chr11:34673863-34673878CGATGACTCATCAGT+6.2
SPI1MA0080.4chr11:34674274-34674288TCCTTCCTCTTTTT-6.06
SPICMA0687.1chr11:34674274-34674288TCCTTCCTCTTTTT-6.38
ZNF263MA0528.1chr11:34674690-34674711CCTTCCATCCTTCCATCCTTC-6.12
ZNF263MA0528.1chr11:34674698-34674719CCTTCCATCCTTCCATCCTTC-6.12
ZNF263MA0528.1chr11:34674706-34674727CCTTCCATCCTTCCATCCTTC-6.12
ZNF263MA0528.1chr11:34674714-34674735CCTTCCATCCTTCCATCCTTC-6.12
ZNF263MA0528.1chr11:34674722-34674743CCTTCCATCCTTCCATCCTTC-6.12
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_23244chr11:34673790-34674219Colon_Crypt_1
SE_23244chr11:34674252-34676211Colon_Crypt_1
SE_26655chr11:34670108-34673600Esophagus
SE_26655chr11:34673708-34677938Esophagus
SE_31738chr11:34673056-34673526Gastric
SE_31738chr11:34673765-34676924Gastric
SE_33847chr11:34673660-34677748HCC1954
SE_34914chr11:34672715-34678354HeLa
SE_35339chr11:34673649-34679228HepG2
SE_41618chr11:34673725-34674186LNCaP
SE_41618chr11:34674365-34675073LNCaP
SE_50680chr11:34674352-34676099Sigmoid_Colon
SE_52951chr11:34673750-34676443Small_Intestine
SE_56256chr11:34671428-34679748u87
SE_64547chr11:34674107-34677482NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr113467377834673986
chr113467427434674504
Number: 2             
IDChromosomeStartEnd
GH11I034650chr113467171234673596
GH11I034652chr113467380134678102
Enhancer Sequence
TGGTAAGCTG TCATCACATC TGAGGCTGGG TATGCCTAAT GCTTAGGGAG AATCAGTGGG 60
AATTACCAAC ACTCTACATT TCTGCCTTTC TGGAGTCTTT CTAATTAAAG GGCTAGGAAA 120
GGGATGGGGT TACCATTAGA CGAGGTTTGC TTTTGAGGCA ATATTTGTAC ATCGAAGATG 180
ACCCGTAGGG ATCCTCTAGG CAAAATGTTG GTCTCCTACG AAACTAGTCA CTCTGTTGTG 240
ACAATAAAAG TTGTTTAGGC TTTTCTTTAT TTTCAATGAA AACTTACTCT TGCAATATAG 300
CTGCTAAAAT TATTCATATT TGGGTATACT TATGGGAAAT AAGGCTATAT TTAATTTTCA 360
ACAAACTACA TTTGGCTTTA GAGAAAGAAT ACCTCATAGT AAAATTCAAA GGTCCGTGAA 420
CCTGTAGTGA TAGTTTCTGG GTGAAGGGGT AGCCATTGGA AACTTCCAGA ATCCCCACAG 480
TTACACTATT TTGTCAGTTT TTAAGTCTAA TTCCGATGAC TCATCAGTGC TCTCTAATCA 540
GTCAGAGCAC CTGCATTTTA TGAGTTACGT TCACTTTAGC TGCATTTGGT TAAGCTTGGA 600
TGCAACTGGG GCTATCCATG CTCCTTAACC AAGGTTACAC TGGGTGAGAA GTTTGGGATG 660
TTGGGAGTCT GGGAGAGGGG ATTTCAGATT ACCACCCCCA CCTACAAATA GGTGCATTGG 720
CGTGTACAGT GTGGGAAATG GTTGAAAGAG GATCTTATGG TTTCCCGTGA TCTGAGTATG 780
AACTTGTGGA TCTCTTTGGG TCTATGAAAT GGCACTTAGA CATCAGTCAC AAGTGATAGT 840
GCCTCTCTCC TGGAATTAAA TTTGGAGCAA CTTCAGAAAT GGGATTTAAT TGGGTCTTTG 900
TGAAAGAAAT TAGTCTGCAA CCCTTCCTTC CTCTTTTTTT CTGTTTTTGT TTTTGCTTTT 960
GAGAACTGAA ATAATGAAAG GTTTTGGTTT GAGGTTTTGT TTGGGTCAAG CCCCTTAAAT 1020
GAGATGGGGC TGGGAGCCAA TGTAAATGCT TCTGGAATTG AGATTAAGAG CTGAGGCCAG 1080
CATAGCTCTC GACTTCTCCT TCCCCCAGTG GTCCTTAGCA TTATGTGTCA CTTGAGGTAT 1140
TTGTTAAAAT TAGGGAATAG ATCAAACACT GGCAAGGCTT GGCTGTGTAT TTGCTATTCT 1200
GGGGGAACTG AGCCAACCGG GGTAAAATTT CTGTGGCAAT CATTGCCACT CAGTCAAGAC 1260
CATGGGGTTC AGGGCTGAGG AAACCTCCCA AGTCACACTC TGAGTTCCTC TGCGACTTCC 1320
TACAGTGTCA TCTCCCACAT CCTTCCATCC TTCCATCCTT CCATCCTTCC ATCCTTCCAT 1380
CCTTCCATCC TTCCACTTGG GTCTTTGACT TACGGCAAAA AATTCCAACT AAGAATAAAG 1440
CTGAACCAAC 1450