EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-19641 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr17:76338030-76340470 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr17:76338069-76338080GGGGGCGGGGC-6.02
KLF5MA0599.1chr17:76338070-76338080GGGGCGGGGC-6.02
RFX2MA0600.2chr17:76338277-76338293GGTTGCCATGGCCACG-6.14
RFX2MA0600.2chr17:76338277-76338293GGTTGCCATGGCCACG+6.35
RFX5MA0510.2chr17:76338277-76338293GGTTGCCATGGCCACG+6.59
RFX5MA0510.2chr17:76338277-76338293GGTTGCCATGGCCACG-6.6
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00808chr17:76338385-76338759Adipose_Tissue
SE_02705chr17:76337594-76340092Astrocytes
SE_06650chr17:76338038-76341562Brain_Hippocampus_Middle
SE_17289chr17:76338035-76338733CD4p_CD225int_CD127p_Tmem
SE_17289chr17:76338803-76340512CD4p_CD225int_CD127p_Tmem
SE_17631chr17:76337551-76342210CD4p_CD25-_CD45RAp_Naive
SE_19096chr17:76338464-76341414CD4p_CD25-_Il17-_PMAstim_Th
SE_19802chr17:76338054-76340533CD4p_CD25-_Il17p_PMAstim_Th17
SE_26074chr17:76338090-76340305Duodenum_Smooth_Muscle
SE_26825chr17:76337371-76340379Esophagus
SE_29662chr17:76337974-76340513Fetal_Muscle
SE_31461chr17:76335686-76340372Gastric
SE_34272chr17:76337488-76342310HCT-116
SE_34704chr17:76336643-76340393HeLa
SE_36965chr17:76337036-76340497HSMMtube
SE_38941chr17:76338135-76340469IMR90
SE_40802chr17:76337300-76340350Left_Ventricle
SE_42104chr17:76336058-76340432Lung
SE_44143chr17:76338074-76340415NHDF-Ad
SE_44765chr17:76337033-76340417NHLF
SE_45620chr17:76337306-76340402Osteoblasts
SE_46745chr17:76338068-76338789Ovary
SE_46745chr17:76338798-76339984Ovary
SE_47352chr17:76338068-76340526Panc1
SE_48690chr17:76337530-76340186Right_Atrium
SE_50089chr17:76337497-76340480Sigmoid_Colon
SE_51088chr17:76335853-76343308Skeletal_Muscle
SE_51835chr17:76338181-76339927Skeletal_Muscle_Myoblast
SE_52389chr17:76337329-76340411Small_Intestine
SE_53327chr17:76337274-76340434Spleen
SE_55689chr17:76337288-76340447u87
SE_57854chr17:76337512-76338495VACO_503
SE_58926chr17:76309354-76389031Ly3
SE_61360chr17:76309626-76357699HBL1
SE_62409chr17:76309367-76385525Tonsil
SE_63627chr17:76338115-76340165HSMM
SE_65603chr17:76338067-76339984Pancreatic_islets
SE_67525chr17:76337288-76340447u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177633833776338836
Enhancer Sequence
GGACGCGAGG ACCCGGGTGG GCGGGTCCGC GGGCGGGGTG GGGGCGGGGC GCGGGGCCGG 60
GACCGGGATC CCGGGCGCGG GGCCAGCCCG AGGCGGGTGG AGCCGGGCGC TGACCTCACA 120
GCCCGCGAGG AAGCCCGTCG GGGCCGGCGG GGCTGATGGA AGGCCTGAGG AATTCGCAGC 180
CGGCGGCGCG GCCGGGCGCG TTCCCTTCCC CTCTCTCCGT TGCCCGGCGA GGGAGCCACA 240
GCGCAGCGGT TGCCATGGCC ACGGGCCGGG CGTGGGGCTG GGGGACCAGG GGCCGCTGAG 300
CCTCGATCAC CTTGTCCTGC TCGAGCCAGG TTGGCATGGA CTGGAAGAAC CCCGCGGCGG 360
CGGGCGGGAG GTGCTGGGGC CAGGGGAGGC CCCGAGGGAC CCCGCCGCCC GGTCTGCGCC 420
CTGATCCCGC AGGGTCCTGT GGAAATGCGG TGTCTGCCTC CCCGCCTCCT GCGCTCACAC 480
ATGCAGGCCT GGGGCCTGCG GGTCCCGGGG CTCTGAGCCT GCACAGCCCA CGGGCCGCAG 540
CCGCAGGCCC CGCACTGGTA GCTTAGGTGG ACACGGAGGC TGAGGGGGAG TTTCCAAGGG 600
GCCTGGCCTC ACGCTCTGCC CGTCACAGCC GCCACCCCTC ACCGGCCCTC CACCCACCCC 660
TAACTCCTTA ACCTCTCCCG GCCTCGGTTT CCTCACCTAT TAACTAGAGA TTAGTCATAG 720
CTACCATCCA GGCTTGTTAT ATTAAAATAG AATAATTATG TAATGTGCCG TGTGCACTCC 780
AAACGCGGTC CTCTTTCCCT GTCCCACACC TCCTTCCTCC TGCATCAGGC CTGGGGAGGG 840
GGGCGTGCCG ATGTCACCCC CAACCCCCAG GCCTAGAGTC CTGGACACAT GGACGCCCCT 900
GCCAGAGCTC CCCTCCCCGC GCTTGGGGTT ACTTTGAACC CCGCCTCCTA CAAGAGGATG 960
GTCCAGCCTA TTGTCGGAAC CTGCAGGAAT CCCAGGCTGC GACCCAAGAA TATTAGCGGA 1020
GGCCCAGCCT GGCTGGGGTG AGTCAGCCTC TCCTCCCAAA TTCAGTTGCG GCTTCAGCTG 1080
CCCTGTGCAG CTGGGGCTGC TAAGTTGCCA GCAAGAGGCA GCCTCTGAAA ATCTCTGGAA 1140
AGACCAGCAT GTCCTTGGGG TGGGATTCAG AGCACAGTGG GGTGGGGGAG GGTTGAGAAG 1200
GGGTCTTGAT CCCCCTTCTC TTCCTCTAGG GGAGCCGAGG CTTGGGACCA GGGAAGCAGC 1260
GGTACCCCAT GTGGGGAAGG GCGGGCCTGA CTTACTGTAA CTTCCTGGCC CAAAGCCTGA 1320
TTGTCCTGTG GTTGGGCTGC CCGGCCAGAG AGGCCCCTGG TGTAGGGAGG ACTCAGAGAG 1380
AACTTGCCTC CCGTTGCCAG GGCCCAGTGT GTGTGTACTG GGGGGCGGAG GGGCTGTGCT 1440
GTCACTGATT TCCTGAGACA GCTAGTAGAC CAGATGAGGC TGCCTGGAAG GTGGCTCCTC 1500
TTCCCTAAGC AGGTTGGGCC ACTACCTAAA TGCCAGGTTA TTTACAAGAA AAAAAAAAGG 1560
CTGTCCAGGG GCTCAGCCCC TTTTGGAGGG CATCAGAGCC GCCAGTGTTG ACTGAGCACT 1620
CACCATGTAC TACGCCATAT GGGCGTTTGC TCACTGAACT GTCACAACCA CCCAAGAAAA 1680
CGGGAACTGT TGTTATCCCC ATTGTACAGA TGGGGAGCGG ATTTAGAGTC CTGGGATGCA 1740
AACTGGGTTT CCCCGCTGGC TCCCGATCCC CACTCCATCT GGCCTATGAG CGTGGGAACC 1800
AGTGTGGCCC GGAAGAGTGG TGGATGGCCC AGCTGACTGC CCAGGTGCCC CCACCCCCCA 1860
GCCACATGGG CATGCGGCTT GCTCGGTACT CAGCTGACTT CCTGTCCCTG GAAGAGCAGC 1920
TGCCGGTATG CTGGGGCAGG GCGGTCCCCT TCCTGTGGTT CAGGTAAGGG CATAACCCCA 1980
TGCCTTCTTG GCATCCTCCC TCTCTCCTTT CTCAGGCTCT GCAAGTCCGA CCTGGGTGCC 2040
CCAGAGAGCT GCTCCGGGAA AGACGTTTAC CTGCTGCCCA GAGCTGGGAC TGCAGACCCT 2100
GATTGGCGAG GGCTTGGAGA GTAGCTGAGA ACCTTCCCTT CAGCTACTGA AGACCAGACA 2160
GGGCTTTCTG TATCACGCTG CCTGACGATG ATGAGGGTGC AGTGACTAAG AGTGCAGATG 2220
AAAGGCCCAG CTCTCCAACC AGGTGGATGG ATTTGCAAGG AGCTTCTATC TGGGCGTGGT 2280
GGCTCATGCC TGTAATCCCA GCACTTTGGG AGGCTGAGGC GAGCGAACCA CCTGAGGGTG 2340
GGAGTTCAAG ACCAGCCTGA CCAACATGGA GAAACCCCAT CTCTACTAAA AATACAAAAT 2400
TAGCCGGGCA TGGTGGCAGG CACCTGTAAT CCCAGCTACT 2440