EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS120-04138 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr20:43970440-43973400 
Target genes
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr20:43970932-43970947AGGTCAGTCTGTCCC+6.17
EWSR1-FLI1MA0149.1chr20:43971340-43971358GGGAGGGAGGAAGGATGG+7.09
FOSL2MA0478.1chr20:43973046-43973057GGGTGACTCAG+6.02
FOXP2MA0593.1chr20:43970785-43970796ATGTAAACAAA+6.14
JUNBMA0490.1chr20:43973046-43973057GGGTGACTCAG+6.02
ZNF263MA0528.1chr20:43972324-43972345GGGGGATAAGGGGGATGGAGA+6.05
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00964chr20:43964885-43977614Adrenal_Gland
SE_01911chr20:43964890-43978032Aorta
SE_02392chr20:43969504-43977658Astrocytes
SE_23562chr20:43968306-43977650Colon_Crypt_1
SE_24283chr20:43970212-43973779Colon_Crypt_2
SE_26046chr20:43964321-43977082Duodenum_Smooth_Muscle
SE_26791chr20:43964902-43977688Esophagus
SE_28171chr20:43968612-43977361Fetal_Intestine
SE_29157chr20:43968321-43977386Fetal_Intestine_Large
SE_31528chr20:43964178-43978011Gastric
SE_33992chr20:43964899-43976782HCC1954
SE_35002chr20:43964136-43977911HeLa
SE_35976chr20:43963799-43977058HMEC
SE_37725chr20:43971878-43978017HSMMtube
SE_39008chr20:43964972-43977155IMR90
SE_40831chr20:43963949-43977702Left_Ventricle
SE_41658chr20:43968300-43973685LNCaP
SE_42476chr20:43963996-43977803Lung
SE_44639chr20:43970127-43977753NHDF-Ad
SE_44896chr20:43969941-43977366NHLF
SE_45837chr20:43963257-43977959Osteoblasts
SE_47536chr20:43968320-43977079Pancreas
SE_48276chr20:43963617-43978083Psoas_Muscle
SE_48947chr20:43964906-43977636Right_Atrium
SE_49537chr20:43970173-43973703Right_Ventricle
SE_50902chr20:43968274-43977802Sigmoid_Colon
SE_51424chr20:43963960-43978125Skeletal_Muscle
SE_51945chr20:43972279-43973782Skeletal_Muscle_Myoblast
SE_52708chr20:43964889-43977710Small_Intestine
SE_56644chr20:43969982-43977740u87
SE_57011chr20:43970213-43977179VACO_400
SE_58242chr20:43970204-43973793VACO_9m
SE_63737chr20:43972070-43973782HSMM
SE_64465chr20:43964144-43977081NHEK
SE_69070chr20:43968795-43973708H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr204397282143973151
Enhancer Sequence
GGGTGCCAGC TAGAAATGGG GGAAGGGTTC AGGAGCCTCT GGATGTCTCC CTGCCAGGAG 60
CTGACCCAGC ACCCTTGTTA CTAACTCCCT GGATGATCGT GGACAATTCC CTTCTCTGAG 120
CCTCAGTTTT CCAATCTGTA AAAGACAGGT CTCAAAGAGA CAAGCCTCCC TCTGTCCCAG 180
CCCAGTAACC AAGCTGGGCA TTGCTCCGAT TACCGGTGGA GACAGCCAGG AGGGGGCTGG 240
CTCCCTCAGG GCCTCAGAGA CAGAGGTGCA TTGAAGTTGG AGCTTGTAAT CTAGGCAGCA 300
GATCCGAAAT CCCTGCTGGA TCCGAGGGCT AGGGAGGCTC TCGGGATGTA AACAAACCTC 360
CTGTGTTCTC AGAGCAGAGT AGAGAGCCCA CGCTGCAGCC TTATCTCAGC TGATTAGATC 420
AGCCCTGGGT GCTGGCTTCC TGCCTCTTCC CAGCCTCCCT CACCGACCCC CAAGGAAGCC 480
ATCCTCCAGA CCAGGTCAGT CTGTCCCACA GACGGCTCCG GCAGGGCTTC TCCAAGGCAA 540
GGAGTATCCC CACTCTGGGT AGCCGGGCCA GCCATGTGCC ACATCTGCCC CCACGCCCAG 600
AGGCTAGAGT GACACCGCCA GTCCCCGCAG GCCTGGCCAC TGACTGCTGG GCTTCACCAA 660
GTCACTGTTT CCACACATAC CAGCCTCTCC CTGCCTCCCC TTTCCATTAC CCCAGGTGTC 720
ACCTGACCAG CAGCCTCTTC TACTGTGCCA GAGAAAACTG GAGCAGCCGA GCTCCCGGGC 780
CTGGAGGACA GGGGGAGGGG TGAGATGCAG CCTGAAGGGG TGGGGGCCGC TGAATAGGAA 840
GGTCTGGGCT GAAGGTGGGG GTTGGGGGAA GCAGGAGGCA AGAACAAGGC TGGGAAGTGG 900
GGGAGGGAGG AAGGATGGCT GTAGAAAGGT CAAAGCCAGA AAGAACTGCT GAGATCAGAG 960
TGACCTTTTG GGGAGTACTG CAGCCCCCTG AAAAGGATAA AAAGGTCTAA ACCCCAATAA 1020
CTGTAACTCT TAGTTTACAT TTTCAACATA TGCACAGACA CCACCTCCCC AAAGCCAAAC 1080
TCTGGCCGGG TTAAGAACCC TCGTCTAGGT GCTAATAAAG CCAGAACTTT ACAAGTTTGC 1140
CAAACAGCGA TGATGACCTT TGAGTGCCAC AGGTGTTTTA TAGAGGACAC TGGAGTTCAC 1200
ATCAACAAAG TGACGTATTA ACTGTGTGTG TCCCTGGGTG AGCAGCAGAG CTAGGACGGG 1260
GGCTGGAGTT TTCTGTACCC TCTTTTTCAG TCACCCAGCC TTCAGCAGAT GGGACCAGAG 1320
AGGCCCCAGT GAGATGCAAG AATGTGCCCA AGGTCACCAC TGTGTTAGTT AATGACAAAC 1380
AAGCCCAAGA AGTCAGGCTT ATTCTTCTAA GGTTAAATGA GACCCCAACT GTTGACATAT 1440
GTGTTCTCTC TCCTCCCTCT CTAGGGCACC ATGCAGTGAA AACATACGAG AAACTGGCTT 1500
TTCAGAACAC TGTACCTTTT CTGTCCACCA ACACCCCACC CCTCAAAGTG CTATTTGCAA 1560
TCACTCAGCC TCCTTAAGGG TAGAAACTCT GCCCCTCCAG CACAGGAGGG TGACCCCAGG 1620
TCCTGGACAG TGTCCAGAGT GGTCTGATAC CCTTGGCAAA CCCCCTGCCC CCTCTCCCTC 1680
CAGGCTGCAA ACTGTTCAGC ATGAGGCTCC AGCAAATCCC AGCAGGAGAG GTGGGGCTGC 1740
CCAGAACTGG TTCTTGTTTA AACATAAACC CATTCGATAA TTAGCAAACA GCCCACTTCT 1800
AAGATAAACA AATAGGAGAT TTGGACTCCA AAAGCCCCAC CCTAGATTTC TCCCTTCCCA 1860
CCTCCCAGCT GTGGGGGTAG ATAAGGGGGA TAAGGGGGAT GGAGAAAGCT TTCCAGGAGA 1920
CCTGGGCTCA GAATCTTCAG AGATAGGACC CCCTGGCATG AAGGTGGCCT GGGCAAGGAA 1980
GGGAACTGTC ACTAAGTAAC ACCTCCTCCC TACCAGGCAT GGTACTAGGT GCCTTTATTT 2040
ACAGCCCTGT CGTCTCCTTT AAGCTTCGCC ACACCGGTAT CATGATCTTC TTAACAGACC 2100
AGGAGGCTGG GGCTCAGAGG TGGAGTAGCA TGACTGAATT CATGTAGCCA GTAAGAGGTG 2160
GACTTCGCAC GTCTGGAGTT AAGTCTGTGT AACACCAAGC CAATGTTTCA ATGCCCTCTG 2220
GCCAGCCCCA GGAAGCAAAG AGGAGTCCTC ACAAACATCA GAAAATCCTG GGGTCACACC 2280
AAACCTGAAC AGTACCAGCT TTTGCTCTCT GAAAAAATGC AGGCCAGTTG CAGCCTCAGT 2340
TTTGCCTTAA AGAGGAAAAA AGTACTACCT GCTCTGCAGA GGTCTAAAGC CCAATTTTGA 2400
GGACTGGCTG CACAATGTAC AATGTCAAAG TCTACATGCA GGCAAGGGGC TGTGAAAGTG 2460
CGGGACCTAG TACAAACATG TCCTGTATGT CCCCTCGAGC CCCGGACACT GAAACAGTGA 2520
CTCCCAAAGG ACAAGGTAAA ACTCTGAGCT CATTCCAACA CCCCCACCAC AGAGCTGTCC 2580
TATTAGCCAA GAGTTTGAAA GGAAATGGGT GACTCAGGCA GGCTACGCTA GCATGCAGTG 2640
ACTCACAGCG CTCGGTCCAG CCCCTTACCC CAATTTTAAG CATTCATTTG GAAATCACAC 2700
TCGCCTGTCC AGTCCGGGAG GTTGAAGGAC AGCTAGGAGC CAACTTCTCC CAACAGGGAG 2760
ATGGGGCTGG GAGCCCAGCC TGGCTTCCCC AGCTCCTCAT TCAGGCAGGC TCAGCACTCC 2820
AAGTCCTTGG AAAAGCCCTC TGTTTCTAGG AGCTGGGGAT GGCAGGAGCT GAATGTCCCC 2880
CCGCCACCCC AACTTCTCTT CTGAGACTGG GATTTGTTTA GACTCTTCAC CAAGGAGGCC 2940
AGCAAAGGGC CCCTCCCCTC 2960