EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS102-19655 
Organism
Homo sapiens 
Tissue/cell
HuCCT1 
Coordinate
chr6:41690550-41692280 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs13200335chr641690823hg19
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: 33             
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_42849chr6:41690562-41693465Lung
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
AAGTGTTAAC CTGTGCAGGC ACTTAGTGGG AGGCTGGCTC TATTCTGAGC ACTTTATGTG 60
AGTAAAGTCT TTTACTCTTC AGAACTCACA AGGTGGGCAC TATAACTGTC ATCTCCATGT 120
TACAGATGAG GAAGCAGAGG AGGATAACTT GCCAGCATCA TGAAACTGCA AAACGACAGG 180
GCCAGGATTC AAGCAGGTGG ATGTAGAGCA TATGCTCCCA GCCCCTAATG TAAATGGGTA 240
TTCACTGTGG CCTGGCCAGT GACATGCTAA GCCCATCCTG CCCATGACCT TCTCACTCGA 300
CCCTTGAAAT AAGCCTGGAG AGATGAGGAA ACTGAAGCAC AACTCTGGCT GACTCCTGAT 360
TTCCCACGCT GTCCAACCTG CACTCCAGAG CTTGGCCACC TTCTTCCCCA TTCTTTCCCT 420
CACCCCAGCC TTGGCCATGC TCAGAGACCC CCACCCCTCC CCAAAGACAT CCCAATGCCA 480
GTGCAGCCTG AGGGGCCTCA TCCCTACCCA CCCACCTCCC CAAAGACACC ACACGCATGC 540
ACATACACTC ACACAGATGC ACACAGGCTA ACACACATGG ACACACATTC ACACACATGC 600
TCACACACAT GCACACACTC ACACACATGC ACGCGTGTGC TCTCATACCT TCGAGAGGGC 660
AGCCCCCTGG AAGGAGGCCC CTGGAATGCT CAGCTCCTCC AGGGGCCGGA GCCCAGGGCC 720
GCACCCCAGC CCCAGGGCCG GGCTCAGTTT CCTCATTTCC CCGGCGGCTG CTGTTTCTCA 780
CCCAGCCCCC TGCACCTCAG CTGGAGAGGA AGTTGCACAA TCCCCTGGGA GCTGCAAATG 840
CGGCCGAGGA TTACTCACAG CACAGAGGGA ACTGCGCCCC GACGGCACAG TCCCACACCG 900
CAGCCTACCC AACACAGACT GCTTCAATCT CACCCGCCCG GCTCCAGGCG CCCACAGCGC 960
TCCTTGGTCC TCCCACAGGA GGCCTCTCAT GGCCGCCCTG ACCCCAGCCT GACCTCAGAG 1020
GGCCCTAGGC AGATGGAGAG ACACAGAGCA GCAAGAATTT CGCCAGAGTC CCAATCCCAC 1080
CAGGTCCAGG GTGGGCCTAA CCCTAACCCC AGCCCCGCTT CCTAGAGACA TGTGTCCTTC 1140
TAGCCAGAAG CCCCACAGCT CACCATCTTC CTGACTGGCC ATACACCTGC AGTCTTGGCC 1200
TTGGGCCTTC CCAGGGCCTC CAGACACCCA GGTCGAGGCC GTACTACAGC CCACCTTGAA 1260
ATGGAGCCTG AGATCAAGCA GAGCCCTGGG CAGCTCCGGG AAGATCCACA CCACCGCACA 1320
CTTTTCACTT GTGCAGAAAC TGTTCTTGAT ACACATGCAA GTTCAGTGGT TCCTCAGCCC 1380
CCCAGCACTT TTTTAGCAGC CTGCCAAAGA GACTGGGCAG AGATTTCACT TAGTGCTTCT 1440
TTCTGGTGGC CAAGGGATTC CCATCGTTGA TAAGCAAATA CCCTGTATTA AGAAAGGTTA 1500
AGCTATTATC GGTCGTCTGC GTCTCAGGGT GGATGAGTTT ACTGGGCCCT TTCGTGAGTG 1560
CAGGTTTCAG GAAGGAAGCG GGCAGCAGAG AGGAGATGAG GCAGGCCGTG GCTCCTGGAG 1620
AAGGCAGGAG ATGCCAGCAA TGTGAGGGAA GCCCAGAACA GTGAGGCCAG AGAGGCCCAG 1680
GGAGGATGGA CCCAGACTCT GGTCCAACCC TGGGCCTCCC TGGGCTGGCA 1730