EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-68946 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr6:41690690-41692840 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs13200335chr641690823hg19
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
AGGATAACTT GCCAGCATCA TGAAACTGCA AAACGACAGG GCCAGGATTC AAGCAGGTGG 60
ATGTAGAGCA TATGCTCCCA GCCCCTAATG TAAATGGGTA TTCACTGTGG CCTGGCCAGT 120
GACATGCTAA GCCCATCCTG CCCATGACCT TCTCACTCGA CCCTTGAAAT AAGCCTGGAG 180
AGATGAGGAA ACTGAAGCAC AACTCTGGCT GACTCCTGAT TTCCCACGCT GTCCAACCTG 240
CACTCCAGAG CTTGGCCACC TTCTTCCCCA TTCTTTCCCT CACCCCAGCC TTGGCCATGC 300
TCAGAGACCC CCACCCCTCC CCAAAGACAT CCCAATGCCA GTGCAGCCTG AGGGGCCTCA 360
TCCCTACCCA CCCACCTCCC CAAAGACACC ACACGCATGC ACATACACTC ACACAGATGC 420
ACACAGGCTA ACACACATGG ACACACATTC ACACACATGC TCACACACAT GCACACACTC 480
ACACACATGC ACGCGTGTGC TCTCATACCT TCGAGAGGGC AGCCCCCTGG AAGGAGGCCC 540
CTGGAATGCT CAGCTCCTCC AGGGGCCGGA GCCCAGGGCC GCACCCCAGC CCCAGGGCCG 600
GGCTCAGTTT CCTCATTTCC CCGGCGGCTG CTGTTTCTCA CCCAGCCCCC TGCACCTCAG 660
CTGGAGAGGA AGTTGCACAA TCCCCTGGGA GCTGCAAATG CGGCCGAGGA TTACTCACAG 720
CACAGAGGGA ACTGCGCCCC GACGGCACAG TCCCACACCG CAGCCTACCC AACACAGACT 780
GCTTCAATCT CACCCGCCCG GCTCCAGGCG CCCACAGCGC TCCTTGGTCC TCCCACAGGA 840
GGCCTCTCAT GGCCGCCCTG ACCCCAGCCT GACCTCAGAG GGCCCTAGGC AGATGGAGAG 900
ACACAGAGCA GCAAGAATTT CGCCAGAGTC CCAATCCCAC CAGGTCCAGG GTGGGCCTAA 960
CCCTAACCCC AGCCCCGCTT CCTAGAGACA TGTGTCCTTC TAGCCAGAAG CCCCACAGCT 1020
CACCATCTTC CTGACTGGCC ATACACCTGC AGTCTTGGCC TTGGGCCTTC CCAGGGCCTC 1080
CAGACACCCA GGTCGAGGCC GTACTACAGC CCACCTTGAA ATGGAGCCTG AGATCAAGCA 1140
GAGCCCTGGG CAGCTCCGGG AAGATCCACA CCACCGCACA CTTTTCACTT GTGCAGAAAC 1200
TGTTCTTGAT ACACATGCAA GTTCAGTGGT TCCTCAGCCC CCCAGCACTT TTTTAGCAGC 1260
CTGCCAAAGA GACTGGGCAG AGATTTCACT TAGTGCTTCT TTCTGGTGGC CAAGGGATTC 1320
CCATCGTTGA TAAGCAAATA CCCTGTATTA AGAAAGGTTA AGCTATTATC GGTCGTCTGC 1380
GTCTCAGGGT GGATGAGTTT ACTGGGCCCT TTCGTGAGTG CAGGTTTCAG GAAGGAAGCG 1440
GGCAGCAGAG AGGAGATGAG GCAGGCCGTG GCTCCTGGAG AAGGCAGGAG ATGCCAGCAA 1500
TGTGAGGGAA GCCCAGAACA GTGAGGCCAG AGAGGCCCAG GGAGGATGGA CCCAGACTCT 1560
GGTCCAACCC TGGGCCTCCC TGGGCTGGCA AATTCTGGAA GGACACAAAG GATGAGTAGG 1620
AGCCAGGCCT GGGTGTGCAG AGCCCCCAGG GAGGACCTCT GGCTCCCGCC CCTTGCCGCC 1680
CGAGACCTGC AATGGGGCCT CAGATAAGGA ACATGATAAA TACCTCTTAT CACCCCCACA 1740
ACCTTGGACT CCCATCCAGC TAAGGACAAA GTTGGAAATG TTTTTGTCCT GGGCCCCAAG 1800
GCTCCCAGAG AACCCCTCAT TTCTGCAGCC CTCATCAAAA GGCTGGGGCC CGCAGGGACT 1860
GTGGGGGAAG CGCCTCACAG CCCCTGCAGC AGCACGAACC AGGACTGAGG TTCACAGCGG 1920
TCACCTGATG CCTCCAGCTT GGTGGACAGG GAACACAGTC AAGGAAGAAG GGCCAGTGCT 1980
GAAAAGGCCT GGCTCTACTG GAACGCAACA GCCACAAGGC CCCTTTGCAG GGACGCCTCC 2040
CCCAAAATGC CTGCACATTC ACCATCTCCC CCATCCTGAC AAGAGCCCCA TGAAGGGGAA 2100
GGGCAGCAAC GCTTGCTATC CGTTTTTCAG ATTCCAAGGA GGCTGAGGCT 2150