EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-20665 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr6:41691010-41693220 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4711689chr641692812hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RARA(var.2)MA0730.1chr6:41691548-41691565TGACCCCAGCCTGACCT-6.85
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_01517chr6:41690972-41692916Adrenal_Gland
SE_03162chr6:41690020-41691233Brain_Angular_Gyrus
SE_03162chr6:41691372-41693461Brain_Angular_Gyrus
SE_03890chr6:41689883-41693577Brain_Anterior_Caudate
SE_04788chr6:41686998-41693888Brain_Cingulate_Gyrus
SE_05789chr6:41686984-41693922Brain_Hippocampus_Middle
SE_06686chr6:41686810-41693790Brain_Hippocampus_Middle_150
SE_07757chr6:41689786-41693648Brain_Inferior_Temporal_Lobe
SE_08794chr6:41691885-41692111Brain_Mid_Frontal_Lobe
SE_10407chr6:41689903-41693737CD19_Primary
SE_10977chr6:41658732-41703851CD20
SE_20329chr6:41689981-41703529CD56
SE_24100chr6:41691488-41691862Colon_Crypt_2
SE_27512chr6:41690300-41692001Esophagus
SE_27930chr6:41686945-41704088Fetal_Intestine
SE_28789chr6:41686934-41704233Fetal_Intestine_Large
SE_32569chr6:41687122-41693433GM12878
SE_40921chr6:41690021-41693217Left_Ventricle
SE_42065chr6:41690065-41691404LNCaP
SE_42065chr6:41692452-41692943LNCaP
SE_42849chr6:41690562-41693465Lung
SE_47896chr6:41692170-41692494Pancreas
SE_48161chr6:41687013-41693572Psoas_Muscle
SE_48786chr6:41690011-41693397Right_Atrium
SE_49598chr6:41690896-41691874Right_Ventricle
SE_50457chr6:41690005-41693468Sigmoid_Colon
SE_51489chr6:41690441-41693523Skeletal_Muscle
SE_53720chr6:41690176-41693495Spleen
SE_58883chr6:41671378-41704020Ly3
SE_59865chr6:41670633-41703769Ly4
SE_60547chr6:41671030-41704212DHL6
SE_61043chr6:41671264-41704230HBL1
SE_61929chr6:41668086-41703943Toledo
SE_62316chr6:41671424-41703890Tonsil
SE_65465chr6:41689674-41693735Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr64169200041692179
Enhancer Sequence
CCAAAGACAT CCCAATGCCA GTGCAGCCTG AGGGGCCTCA TCCCTACCCA CCCACCTCCC 60
CAAAGACACC ACACGCATGC ACATACACTC ACACAGATGC ACACAGGCTA ACACACATGG 120
ACACACATTC ACACACATGC TCACACACAT GCACACACTC ACACACATGC ACGCGTGTGC 180
TCTCATACCT TCGAGAGGGC AGCCCCCTGG AAGGAGGCCC CTGGAATGCT CAGCTCCTCC 240
AGGGGCCGGA GCCCAGGGCC GCACCCCAGC CCCAGGGCCG GGCTCAGTTT CCTCATTTCC 300
CCGGCGGCTG CTGTTTCTCA CCCAGCCCCC TGCACCTCAG CTGGAGAGGA AGTTGCACAA 360
TCCCCTGGGA GCTGCAAATG CGGCCGAGGA TTACTCACAG CACAGAGGGA ACTGCGCCCC 420
GACGGCACAG TCCCACACCG CAGCCTACCC AACACAGACT GCTTCAATCT CACCCGCCCG 480
GCTCCAGGCG CCCACAGCGC TCCTTGGTCC TCCCACAGGA GGCCTCTCAT GGCCGCCCTG 540
ACCCCAGCCT GACCTCAGAG GGCCCTAGGC AGATGGAGAG ACACAGAGCA GCAAGAATTT 600
CGCCAGAGTC CCAATCCCAC CAGGTCCAGG GTGGGCCTAA CCCTAACCCC AGCCCCGCTT 660
CCTAGAGACA TGTGTCCTTC TAGCCAGAAG CCCCACAGCT CACCATCTTC CTGACTGGCC 720
ATACACCTGC AGTCTTGGCC TTGGGCCTTC CCAGGGCCTC CAGACACCCA GGTCGAGGCC 780
GTACTACAGC CCACCTTGAA ATGGAGCCTG AGATCAAGCA GAGCCCTGGG CAGCTCCGGG 840
AAGATCCACA CCACCGCACA CTTTTCACTT GTGCAGAAAC TGTTCTTGAT ACACATGCAA 900
GTTCAGTGGT TCCTCAGCCC CCCAGCACTT TTTTAGCAGC CTGCCAAAGA GACTGGGCAG 960
AGATTTCACT TAGTGCTTCT TTCTGGTGGC CAAGGGATTC CCATCGTTGA TAAGCAAATA 1020
CCCTGTATTA AGAAAGGTTA AGCTATTATC GGTCGTCTGC GTCTCAGGGT GGATGAGTTT 1080
ACTGGGCCCT TTCGTGAGTG CAGGTTTCAG GAAGGAAGCG GGCAGCAGAG AGGAGATGAG 1140
GCAGGCCGTG GCTCCTGGAG AAGGCAGGAG ATGCCAGCAA TGTGAGGGAA GCCCAGAACA 1200
GTGAGGCCAG AGAGGCCCAG GGAGGATGGA CCCAGACTCT GGTCCAACCC TGGGCCTCCC 1260
TGGGCTGGCA AATTCTGGAA GGACACAAAG GATGAGTAGG AGCCAGGCCT GGGTGTGCAG 1320
AGCCCCCAGG GAGGACCTCT GGCTCCCGCC CCTTGCCGCC CGAGACCTGC AATGGGGCCT 1380
CAGATAAGGA ACATGATAAA TACCTCTTAT CACCCCCACA ACCTTGGACT CCCATCCAGC 1440
TAAGGACAAA GTTGGAAATG TTTTTGTCCT GGGCCCCAAG GCTCCCAGAG AACCCCTCAT 1500
TTCTGCAGCC CTCATCAAAA GGCTGGGGCC CGCAGGGACT GTGGGGGAAG CGCCTCACAG 1560
CCCCTGCAGC AGCACGAACC AGGACTGAGG TTCACAGCGG TCACCTGATG CCTCCAGCTT 1620
GGTGGACAGG GAACACAGTC AAGGAAGAAG GGCCAGTGCT GAAAAGGCCT GGCTCTACTG 1680
GAACGCAACA GCCACAAGGC CCCTTTGCAG GGACGCCTCC CCCAAAATGC CTGCACATTC 1740
ACCATCTCCC CCATCCTGAC AAGAGCCCCA TGAAGGGGAA GGGCAGCAAC GCTTGCTATC 1800
CGTTTTTCAG ATTCCAAGGA GGCTGAGGCT CAAATCACTT AAGTGACTTC CTCGAGGCCA 1860
TGCAGCAAGT TTATGGCAAA TCTGTTTCCT GGCTCTTTTC CTAGATCAGA GTTTCTCAAC 1920
CTCAACACCA GACACTCAGG GCCAGGTAAT TAGTTACAGG GGCTGTCCTG TGCATTTTAA 1980
GATGTTTAGT GGTATCCCTG GCCAATATCA TCAGACATTG GCAAATGTCC CCTAGGGGGA 2040
CAAAATCACC CCTAGTGGAG AACTACTGCC CTAGAAGCAC CTAAAAGATG GGCACCTGCC 2100
AATTCCAAAT TGAACGGTAC ACCTGCTGAG GGCTCTAGCC TGAGAGTCTC CCCCTCTCCC 2160
CCACCAGATG TGCTAGGCAA GAGGGCCTGA AGGGTGATGG GTACTCTGTG 2210