EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-26975 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr6:41690780-41692790 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs13200335chr641690823hg19
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
TAAATGGGTA TTCACTGTGG CCTGGCCAGT GACATGCTAA GCCCATCCTG CCCATGACCT 60
TCTCACTCGA CCCTTGAAAT AAGCCTGGAG AGATGAGGAA ACTGAAGCAC AACTCTGGCT 120
GACTCCTGAT TTCCCACGCT GTCCAACCTG CACTCCAGAG CTTGGCCACC TTCTTCCCCA 180
TTCTTTCCCT CACCCCAGCC TTGGCCATGC TCAGAGACCC CCACCCCTCC CCAAAGACAT 240
CCCAATGCCA GTGCAGCCTG AGGGGCCTCA TCCCTACCCA CCCACCTCCC CAAAGACACC 300
ACACGCATGC ACATACACTC ACACAGATGC ACACAGGCTA ACACACATGG ACACACATTC 360
ACACACATGC TCACACACAT GCACACACTC ACACACATGC ACGCGTGTGC TCTCATACCT 420
TCGAGAGGGC AGCCCCCTGG AAGGAGGCCC CTGGAATGCT CAGCTCCTCC AGGGGCCGGA 480
GCCCAGGGCC GCACCCCAGC CCCAGGGCCG GGCTCAGTTT CCTCATTTCC CCGGCGGCTG 540
CTGTTTCTCA CCCAGCCCCC TGCACCTCAG CTGGAGAGGA AGTTGCACAA TCCCCTGGGA 600
GCTGCAAATG CGGCCGAGGA TTACTCACAG CACAGAGGGA ACTGCGCCCC GACGGCACAG 660
TCCCACACCG CAGCCTACCC AACACAGACT GCTTCAATCT CACCCGCCCG GCTCCAGGCG 720
CCCACAGCGC TCCTTGGTCC TCCCACAGGA GGCCTCTCAT GGCCGCCCTG ACCCCAGCCT 780
GACCTCAGAG GGCCCTAGGC AGATGGAGAG ACACAGAGCA GCAAGAATTT CGCCAGAGTC 840
CCAATCCCAC CAGGTCCAGG GTGGGCCTAA CCCTAACCCC AGCCCCGCTT CCTAGAGACA 900
TGTGTCCTTC TAGCCAGAAG CCCCACAGCT CACCATCTTC CTGACTGGCC ATACACCTGC 960
AGTCTTGGCC TTGGGCCTTC CCAGGGCCTC CAGACACCCA GGTCGAGGCC GTACTACAGC 1020
CCACCTTGAA ATGGAGCCTG AGATCAAGCA GAGCCCTGGG CAGCTCCGGG AAGATCCACA 1080
CCACCGCACA CTTTTCACTT GTGCAGAAAC TGTTCTTGAT ACACATGCAA GTTCAGTGGT 1140
TCCTCAGCCC CCCAGCACTT TTTTAGCAGC CTGCCAAAGA GACTGGGCAG AGATTTCACT 1200
TAGTGCTTCT TTCTGGTGGC CAAGGGATTC CCATCGTTGA TAAGCAAATA CCCTGTATTA 1260
AGAAAGGTTA AGCTATTATC GGTCGTCTGC GTCTCAGGGT GGATGAGTTT ACTGGGCCCT 1320
TTCGTGAGTG CAGGTTTCAG GAAGGAAGCG GGCAGCAGAG AGGAGATGAG GCAGGCCGTG 1380
GCTCCTGGAG AAGGCAGGAG ATGCCAGCAA TGTGAGGGAA GCCCAGAACA GTGAGGCCAG 1440
AGAGGCCCAG GGAGGATGGA CCCAGACTCT GGTCCAACCC TGGGCCTCCC TGGGCTGGCA 1500
AATTCTGGAA GGACACAAAG GATGAGTAGG AGCCAGGCCT GGGTGTGCAG AGCCCCCAGG 1560
GAGGACCTCT GGCTCCCGCC CCTTGCCGCC CGAGACCTGC AATGGGGCCT CAGATAAGGA 1620
ACATGATAAA TACCTCTTAT CACCCCCACA ACCTTGGACT CCCATCCAGC TAAGGACAAA 1680
GTTGGAAATG TTTTTGTCCT GGGCCCCAAG GCTCCCAGAG AACCCCTCAT TTCTGCAGCC 1740
CTCATCAAAA GGCTGGGGCC CGCAGGGACT GTGGGGGAAG CGCCTCACAG CCCCTGCAGC 1800
AGCACGAACC AGGACTGAGG TTCACAGCGG TCACCTGATG CCTCCAGCTT GGTGGACAGG 1860
GAACACAGTC AAGGAAGAAG GGCCAGTGCT GAAAAGGCCT GGCTCTACTG GAACGCAACA 1920
GCCACAAGGC CCCTTTGCAG GGACGCCTCC CCCAAAATGC CTGCACATTC ACCATCTCCC 1980
CCATCCTGAC AAGAGCCCCA TGAAGGGGAA 2010