EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-29514 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr6:41690460-41693350 
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
TTCCAGCTCA AACTTCCACC ATCAAAAATG ATCGTCAGGA GCCCTGGGCA GTTTTTTGCC 60
ATCTGCACAC AAACATGCTA TGTCCTGGTG AAGTGTTAAC CTGTGCAGGC ACTTAGTGGG 120
AGGCTGGCTC TATTCTGAGC ACTTTATGTG AGTAAAGTCT TTTACTCTTC AGAACTCACA 180
AGGTGGGCAC TATAACTGTC ATCTCCATGT TACAGATGAG GAAGCAGAGG AGGATAACTT 240
GCCAGCATCA TGAAACTGCA AAACGACAGG GCCAGGATTC AAGCAGGTGG ATGTAGAGCA 300
TATGCTCCCA GCCCCTAATG TAAATGGGTA TTCACTGTGG CCTGGCCAGT GACATGCTAA 360
GCCCATCCTG CCCATGACCT TCTCACTCGA CCCTTGAAAT AAGCCTGGAG AGATGAGGAA 420
ACTGAAGCAC AACTCTGGCT GACTCCTGAT TTCCCACGCT GTCCAACCTG CACTCCAGAG 480
CTTGGCCACC TTCTTCCCCA TTCTTTCCCT CACCCCAGCC TTGGCCATGC TCAGAGACCC 540
CCACCCCTCC CCAAAGACAT CCCAATGCCA GTGCAGCCTG AGGGGCCTCA TCCCTACCCA 600
CCCACCTCCC CAAAGACACC ACACGCATGC ACATACACTC ACACAGATGC ACACAGGCTA 660
ACACACATGG ACACACATTC ACACACATGC TCACACACAT GCACACACTC ACACACATGC 720
ACGCGTGTGC TCTCATACCT TCGAGAGGGC AGCCCCCTGG AAGGAGGCCC CTGGAATGCT 780
CAGCTCCTCC AGGGGCCGGA GCCCAGGGCC GCACCCCAGC CCCAGGGCCG GGCTCAGTTT 840
CCTCATTTCC CCGGCGGCTG CTGTTTCTCA CCCAGCCCCC TGCACCTCAG CTGGAGAGGA 900
AGTTGCACAA TCCCCTGGGA GCTGCAAATG CGGCCGAGGA TTACTCACAG CACAGAGGGA 960
ACTGCGCCCC GACGGCACAG TCCCACACCG CAGCCTACCC AACACAGACT GCTTCAATCT 1020
CACCCGCCCG GCTCCAGGCG CCCACAGCGC TCCTTGGTCC TCCCACAGGA GGCCTCTCAT 1080
GGCCGCCCTG ACCCCAGCCT GACCTCAGAG GGCCCTAGGC AGATGGAGAG ACACAGAGCA 1140
GCAAGAATTT CGCCAGAGTC CCAATCCCAC CAGGTCCAGG GTGGGCCTAA CCCTAACCCC 1200
AGCCCCGCTT CCTAGAGACA TGTGTCCTTC TAGCCAGAAG CCCCACAGCT CACCATCTTC 1260
CTGACTGGCC ATACACCTGC AGTCTTGGCC TTGGGCCTTC CCAGGGCCTC CAGACACCCA 1320
GGTCGAGGCC GTACTACAGC CCACCTTGAA ATGGAGCCTG AGATCAAGCA GAGCCCTGGG 1380
CAGCTCCGGG AAGATCCACA CCACCGCACA CTTTTCACTT GTGCAGAAAC TGTTCTTGAT 1440
ACACATGCAA GTTCAGTGGT TCCTCAGCCC CCCAGCACTT TTTTAGCAGC CTGCCAAAGA 1500
GACTGGGCAG AGATTTCACT TAGTGCTTCT TTCTGGTGGC CAAGGGATTC CCATCGTTGA 1560
TAAGCAAATA CCCTGTATTA AGAAAGGTTA AGCTATTATC GGTCGTCTGC GTCTCAGGGT 1620
GGATGAGTTT ACTGGGCCCT TTCGTGAGTG CAGGTTTCAG GAAGGAAGCG GGCAGCAGAG 1680
AGGAGATGAG GCAGGCCGTG GCTCCTGGAG AAGGCAGGAG ATGCCAGCAA TGTGAGGGAA 1740
GCCCAGAACA GTGAGGCCAG AGAGGCCCAG GGAGGATGGA CCCAGACTCT GGTCCAACCC 1800
TGGGCCTCCC TGGGCTGGCA AATTCTGGAA GGACACAAAG GATGAGTAGG AGCCAGGCCT 1860
GGGTGTGCAG AGCCCCCAGG GAGGACCTCT GGCTCCCGCC CCTTGCCGCC CGAGACCTGC 1920
AATGGGGCCT CAGATAAGGA ACATGATAAA TACCTCTTAT CACCCCCACA ACCTTGGACT 1980
CCCATCCAGC TAAGGACAAA GTTGGAAATG TTTTTGTCCT GGGCCCCAAG GCTCCCAGAG 2040
AACCCCTCAT TTCTGCAGCC CTCATCAAAA GGCTGGGGCC CGCAGGGACT GTGGGGGAAG 2100
CGCCTCACAG CCCCTGCAGC AGCACGAACC AGGACTGAGG TTCACAGCGG TCACCTGATG 2160
CCTCCAGCTT GGTGGACAGG GAACACAGTC AAGGAAGAAG GGCCAGTGCT GAAAAGGCCT 2220
GGCTCTACTG GAACGCAACA GCCACAAGGC CCCTTTGCAG GGACGCCTCC CCCAAAATGC 2280
CTGCACATTC ACCATCTCCC CCATCCTGAC AAGAGCCCCA TGAAGGGGAA GGGCAGCAAC 2340
GCTTGCTATC CGTTTTTCAG ATTCCAAGGA GGCTGAGGCT CAAATCACTT AAGTGACTTC 2400
CTCGAGGCCA TGCAGCAAGT TTATGGCAAA TCTGTTTCCT GGCTCTTTTC CTAGATCAGA 2460
GTTTCTCAAC CTCAACACCA GACACTCAGG GCCAGGTAAT TAGTTACAGG GGCTGTCCTG 2520
TGCATTTTAA GATGTTTAGT GGTATCCCTG GCCAATATCA TCAGACATTG GCAAATGTCC 2580
CCTAGGGGGA CAAAATCACC CCTAGTGGAG AACTACTGCC CTAGAAGCAC CTAAAAGATG 2640
GGCACCTGCC AATTCCAAAT TGAACGGTAC ACCTGCTGAG GGCTCTAGCC TGAGAGTCTC 2700
CCCCTCTCCC CCACCAGATG TGCTAGGCAA GAGGGCCTGA AGGGTGATGG GTACTCTGTG 2760
GTTCAGTACC CTCTGGGAAG AGGCTTCTTA GCCCCAGCAG GCACTGCCAC TTAGGGGGTC 2820
TCCCCACAAG ACCAATATCA CCTTCCAACT CCCAAGCTAC ATGCCAACCC CCTTCCTGGC 2880
ATTCAATATT 2890