EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-20924 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr3:129314510-129317390 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9837325chr3129315831hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EN2MA0642.1chr3:129315008-129315018CCCAATTAGC+6.02
RFX2MA0600.2chr3:129316718-129316734GGTTTCCATGGCAATC+6.04
RFX2MA0600.2chr3:129316718-129316734GGTTTCCATGGCAATC-6.04
RFX5MA0510.2chr3:129316718-129316734GGTTTCCATGGCAATC+6.09
RFX5MA0510.2chr3:129316718-129316734GGTTTCCATGGCAATC-6.13
ZfxMA0146.2chr3:129315150-129315164CTGGCCTCGGCCTG+6.07
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00112chr3:129305417-129325570Adipose_Nuclei
SE_00978chr3:129313612-129319284Adrenal_Gland
SE_01893chr3:129313676-129319163Aorta
SE_04322chr3:129310378-129319241Brain_Anterior_Caudate
SE_05345chr3:129310701-129325499Brain_Cingulate_Gyrus
SE_05951chr3:129308023-129325521Brain_Hippocampus_Middle
SE_07365chr3:129310382-129319614Brain_Hippocampus_Middle_150
SE_08750chr3:129311577-129324158Brain_Inferior_Temporal_Lobe
SE_09767chr3:129314862-129320344CD14
SE_25754chr3:129308309-129320001DND41
SE_26494chr3:129314001-129319380Duodenum_Smooth_Muscle
SE_27065chr3:129313676-129319366Esophagus
SE_29874chr3:129310485-129319205Fetal_Muscle
SE_31151chr3:129314599-129316987Fetal_Thymus
SE_31569chr3:129313699-129319812Gastric
SE_33524chr3:129314769-129317750H2171
SE_37506chr3:129314013-129319542HSMMtube
SE_37994chr3:129310132-129325566HUVEC
SE_40701chr3:129308079-129325658Left_Ventricle
SE_42115chr3:129307923-129325621Lung
SE_46476chr3:129310313-129319510Osteoblasts
SE_46996chr3:129313726-129317137Ovary
SE_47266chr3:129310010-129324076Panc1
SE_48609chr3:129310376-129325641Right_Atrium
SE_49818chr3:129314283-129315255Right_Ventricle
SE_49818chr3:129315309-129316984Right_Ventricle
SE_50249chr3:129311586-129319771Sigmoid_Colon
SE_51354chr3:129310040-129325518Skeletal_Muscle
SE_52687chr3:129313665-129319687Small_Intestine
SE_53375chr3:129310325-129320850Spleen
SE_62855chr3:129293187-129347490Tonsil
SE_65523chr3:129313701-129318953Pancreatic_islets
SE_68869chr3:129314894-129320007H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr3129314620129314813
chr3129314793129317365
chr3129314978129316172
chr3129315034129315445
chr3129315678129315871
Enhancer Sequence
GGCGGGTCAC CCAGCTCCAG GGCTTTGAGG TTATCCAGAC CAGCTGGACA CCATCTGGAA 60
GGGCTGAAGC CAGCCAGCCA GGCCGCCCTG AGGGCCAACA CACAGACTGG GCATGATCTG 120
CCCACCCACC CCAAACAGGC ATGGCCTGGA AGGACAAGCC CCAGGCTTAG GTCACAAGCC 180
TGGCTGGATT AAGGACCTAC TGTGTGACAC TACAGCTACT GGGGGCACCT TACAGCCCTG 240
GGGGTGCACG CACGCACACA CACACACACA CACACACACA CTCTTGCTGC GTACCCATTT 300
TACAGATGAG AAAGCTGAGG CTCCTGACTC CTAAGTCTCA CAGCTCTTAC CTCACTATGG 360
GAGGCACCAT CCCCTCTGAA CCTCGGACTC CACATCTGTA AAATAAGACA GCAATAGCAC 420
CCACCACCTA GGGCTTATGG AAGGACTGAG CTCATAGGAG CCTTCAGTGC TAAGCACTGT 480
AGGTGCTCAA TAAATGTTCC CAATTAGCTA TGCAGACCAC GGAGCAGAGG CTCGGGAGCT 540
CCCGAGGACA GGGACAAGCC ACTCCACCGC TTCCTGAAGT CAAAGCATCC GAGGCTGGAT 600
GGGCTACACC GCCCTCACCA AGGACACAGT AGTGGGAGCT CTGGCCTCGG CCTGCTCTGC 660
CCTGGCGCCT GGGAACCACC GCCACAGTCG CTGACTCAAG CAGCCATTGT TTAGTTAGCT 720
GGACGCAGCC CCTAGACACC CAGCTCCCCC TTCATGAAGC TGTTTCTCAT TCCGGCCCGG 780
CCTGGCCCCA TTTCCAGCTC CCCTCCCCCT GGGTCCCAGA GGAGCACAGT GTGGGATGGG 840
CAGCCAGCGG CTCTTCCCTG GCCCAGGGAA AAGGCTTCCC TCCCCCCAGC AGGAGGGGCA 900
GAGCACGAAG CCAGTCTTTC CAAGCCCTGG AACAGTTTCC CTCCCAGCTT CCTCCCCTGA 960
AGGGACTCCA GGCCAGGAGC CGAGAAATAG TTGCCTCTCC AGGGAACACT GGCAGTTCCC 1020
TCCTGGGGCT GGGGGGACTT GGAGGTTCGA TCTCACACCC TCCTCCCCAG CCCCTGGTCT 1080
CCTCGGGGTC CAGCCCATAT GCCTGGCCGC AGGCTGTGCT CTGCAGCAGG ACTCTACCGC 1140
TGGTCCCAGA GTCATCGCAC GACCGCTGTG GACACAGCCA AGAAGACAGG GCTGCTTGGA 1200
GCCTTGCGCA AACATCTCCG GGCTGGATTC CATGAGCTGG GGACACAGAG GTGACAACGG 1260
GGCCCTCTCT CCAGCTGCCC ACATCCGAGC TCAGAGGCCC AGCCCCAGGA TGGGGAGGGG 1320
CAGCTTTCTC ATAGTAACAG TTCGGTAGAG TGACAGTAGC AAGCAGCTGT GTGCAGTCTG 1380
CTTTGTGCTG AGACCTCTTT CTGTATTATC TCATTCAACC CTCACCACAC CCTGAAAGAG 1440
TTGATGCTGC TTTACAGTAA AGGAAACTGA GGCACAGAGA GTTGAAGTGA TTTGCCCAGG 1500
GGCACACAGC CGGAATGGCT AGATCCAAGC CTCCAGCGCA GGCCTGCGGG CTCCAGATCC 1560
CCGCCCTTAA CCACAGCCTC CCCACCCGCC GCTCTGCTGG GAGCCACCAA TGGTTGCCAG 1620
GAAATCAGCC GCTTGGAGCT GGAAAAACCC TGGGTTTTGA GCTGGGGAAA CTGAGGCCCA 1680
TCAAGGTGAT GGCTGCTTCT AGAGAGCTCA GTCACCTCAA ACAAAGATAG CGGGCAGAGG 1740
CTGGAGAAGG GCACAGGCAA GGGGGTTTGG CCACTTTCCT GGGCCTGGCC TCCACTCCAA 1800
GGCCTCTGCC TGCGGGCCCC CCCCCATTAT TTACCGATCA GAGCATAAAG TGCTACATGA 1860
TTAACGCCCC ACTGGGGCCT TGCCGGGACT CGTAATGGAG CTGCGAGCTT CCCTCCCCCT 1920
CCAGCGCATG ATTTATCAAG TTTCAGGGTA AAGGACGGTG GACTAGGCGG GGAGGGCCCC 1980
CGCTGGCGCT GGCCCCCAGA TCTTGACTGC ATCGAGTATC AGCCGAGCAG GGTGGAGCAG 2040
GGCCCCTGCC ACTGGATGCC TGTCTGGGCG GTCTGTTTGG TTCGGCCCTG GCTCAGACAT 2100
GGCCTTTGGA AAGAAGAAAA CGGCTGTACT TGGGGGGCAG TGAGGATCCA AGTCCACGTG 2160
GCTGGCACTC AGAGACTTTC TGGGCTTGTC CCCACTCGGG AACCGGCTGG TTTCCATGGC 2220
AATCCCCACA TGGCTGTCAG AGCTGGAGAG GCCCTCGGGA GTTACCTGGT CCAGCCACAG 2280
TGGGGGCTCC GGGTGAGCGC CTCCGCCCCT GGATCCTGCC AGCACCTGGC AGGGCCAATA 2340
CAGACCAGCA GCCACAGGGT CCCTTCCGGA ACCAGATCAG CCATGTCTCT CCTTTCCCCA 2400
AAGCCCTGCT GGCTCCCCGC AGCCCACATG ACAGCATCCA AGTCTTTAGC CTGCAGGCAA 2460
GGCCCAGCAC ACTCTCAGCT TCCCCTCGGC CTGCTACCCA AGCCACATTC CAACATCTCT 2520
GAGCCTTTGC CCCTATCGTG TGCTCTGCCT GGAATGCCTT CCCCAGCCCC ATCTGTCAAG 2580
TGCTGCTCCA ACCTCCCCTC CTCCAGGAAG CCCTCCCGCA CTCCTCTGAT GAGCTGGTTA 2640
GTGTGTGGCA TCTGTCTGAT GTCATGACCT CCTCCCTCAC CATTCTGGGG GCTCCTGGAG 2700
AGGGTCCAAT TTGTCTCTCT TGGGGGCTGT CCTGTAGCAA GCTGAGCCTC CTCCCATACT 2760
CACATACTCT AGAGAGCTCC CCACCCAGAG CTTGGACGGG CATGCGATGT TACCAAGGAG 2820
GTGCTGGCCT CTGGTATGTG TGGGTGGAGA CAGCTACAGG CCCGGTAGCA GGAGTCCACA 2880