EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-34216 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr6:41690170-41692940 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs13200335chr641690823hg19
rs4711689chr641692812hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RARA(var.2)MA0730.1chr6:41691548-41691565TGACCCCAGCCTGACCT-6.85
ZNF263MA0528.1chr6:41690673-41690694AGATGAGGAAGCAGAGGAGGA+6.16
Number of super-enhancer constituents: 34             
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_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
CCTCTCCCAT ACTTCTATTG GAACCCAGAA AAGGGGCAGG GGTGTGGGTG AGGGGCCCAC 60
CTGTGGGCTG AGTGGACCAT TCTGCCATTC TCCCTCACTG ATATAGCTGC CCTGGAGCAA 120
GTCACTCTAG CCCCTGGGCC TACATGTCCC CATCTGCAAA ATGGGAATGA TAGCAGCATC 180
CCCCTCATGG GGTGACTGAG GGTGAAGGGG CTGGTACAGA TGAATCACTG GGCACAGTAC 240
CTGACATGGA ATAAGGCCAG GTAAACATGA GCTCTTACTA TCAATCTCAG TTCCAGCTCA 300
AACTTCCACC ATCAAAAATG ATCGTCAGGA GCCCTGGGCA GTTTTTTGCC ATCTGCACAC 360
AAACATGCTA TGTCCTGGTG AAGTGTTAAC CTGTGCAGGC ACTTAGTGGG AGGCTGGCTC 420
TATTCTGAGC ACTTTATGTG AGTAAAGTCT TTTACTCTTC AGAACTCACA AGGTGGGCAC 480
TATAACTGTC ATCTCCATGT TACAGATGAG GAAGCAGAGG AGGATAACTT GCCAGCATCA 540
TGAAACTGCA AAACGACAGG GCCAGGATTC AAGCAGGTGG ATGTAGAGCA TATGCTCCCA 600
GCCCCTAATG TAAATGGGTA TTCACTGTGG CCTGGCCAGT GACATGCTAA GCCCATCCTG 660
CCCATGACCT TCTCACTCGA CCCTTGAAAT AAGCCTGGAG AGATGAGGAA ACTGAAGCAC 720
AACTCTGGCT GACTCCTGAT TTCCCACGCT GTCCAACCTG CACTCCAGAG CTTGGCCACC 780
TTCTTCCCCA TTCTTTCCCT CACCCCAGCC TTGGCCATGC TCAGAGACCC CCACCCCTCC 840
CCAAAGACAT CCCAATGCCA GTGCAGCCTG AGGGGCCTCA TCCCTACCCA CCCACCTCCC 900
CAAAGACACC ACACGCATGC ACATACACTC ACACAGATGC ACACAGGCTA ACACACATGG 960
ACACACATTC ACACACATGC TCACACACAT GCACACACTC ACACACATGC ACGCGTGTGC 1020
TCTCATACCT TCGAGAGGGC AGCCCCCTGG AAGGAGGCCC CTGGAATGCT CAGCTCCTCC 1080
AGGGGCCGGA GCCCAGGGCC GCACCCCAGC CCCAGGGCCG GGCTCAGTTT CCTCATTTCC 1140
CCGGCGGCTG CTGTTTCTCA CCCAGCCCCC TGCACCTCAG CTGGAGAGGA AGTTGCACAA 1200
TCCCCTGGGA GCTGCAAATG CGGCCGAGGA TTACTCACAG CACAGAGGGA ACTGCGCCCC 1260
GACGGCACAG TCCCACACCG CAGCCTACCC AACACAGACT GCTTCAATCT CACCCGCCCG 1320
GCTCCAGGCG CCCACAGCGC TCCTTGGTCC TCCCACAGGA GGCCTCTCAT GGCCGCCCTG 1380
ACCCCAGCCT GACCTCAGAG GGCCCTAGGC AGATGGAGAG ACACAGAGCA GCAAGAATTT 1440
CGCCAGAGTC CCAATCCCAC CAGGTCCAGG GTGGGCCTAA CCCTAACCCC AGCCCCGCTT 1500
CCTAGAGACA TGTGTCCTTC TAGCCAGAAG CCCCACAGCT CACCATCTTC CTGACTGGCC 1560
ATACACCTGC AGTCTTGGCC TTGGGCCTTC CCAGGGCCTC CAGACACCCA GGTCGAGGCC 1620
GTACTACAGC CCACCTTGAA ATGGAGCCTG AGATCAAGCA GAGCCCTGGG CAGCTCCGGG 1680
AAGATCCACA CCACCGCACA CTTTTCACTT GTGCAGAAAC TGTTCTTGAT ACACATGCAA 1740
GTTCAGTGGT TCCTCAGCCC CCCAGCACTT TTTTAGCAGC CTGCCAAAGA GACTGGGCAG 1800
AGATTTCACT TAGTGCTTCT TTCTGGTGGC CAAGGGATTC CCATCGTTGA TAAGCAAATA 1860
CCCTGTATTA AGAAAGGTTA AGCTATTATC GGTCGTCTGC GTCTCAGGGT GGATGAGTTT 1920
ACTGGGCCCT TTCGTGAGTG CAGGTTTCAG GAAGGAAGCG GGCAGCAGAG AGGAGATGAG 1980
GCAGGCCGTG GCTCCTGGAG AAGGCAGGAG ATGCCAGCAA TGTGAGGGAA GCCCAGAACA 2040
GTGAGGCCAG AGAGGCCCAG GGAGGATGGA CCCAGACTCT GGTCCAACCC TGGGCCTCCC 2100
TGGGCTGGCA AATTCTGGAA GGACACAAAG GATGAGTAGG AGCCAGGCCT GGGTGTGCAG 2160
AGCCCCCAGG GAGGACCTCT GGCTCCCGCC CCTTGCCGCC CGAGACCTGC AATGGGGCCT 2220
CAGATAAGGA ACATGATAAA TACCTCTTAT CACCCCCACA ACCTTGGACT CCCATCCAGC 2280
TAAGGACAAA GTTGGAAATG TTTTTGTCCT GGGCCCCAAG GCTCCCAGAG AACCCCTCAT 2340
TTCTGCAGCC CTCATCAAAA GGCTGGGGCC CGCAGGGACT GTGGGGGAAG CGCCTCACAG 2400
CCCCTGCAGC AGCACGAACC AGGACTGAGG TTCACAGCGG TCACCTGATG CCTCCAGCTT 2460
GGTGGACAGG GAACACAGTC AAGGAAGAAG GGCCAGTGCT GAAAAGGCCT GGCTCTACTG 2520
GAACGCAACA GCCACAAGGC CCCTTTGCAG GGACGCCTCC CCCAAAATGC CTGCACATTC 2580
ACCATCTCCC CCATCCTGAC AAGAGCCCCA TGAAGGGGAA GGGCAGCAAC GCTTGCTATC 2640
CGTTTTTCAG ATTCCAAGGA GGCTGAGGCT CAAATCACTT AAGTGACTTC CTCGAGGCCA 2700
TGCAGCAAGT TTATGGCAAA TCTGTTTCCT GGCTCTTTTC CTAGATCAGA GTTTCTCAAC 2760
CTCAACACCA 2770