EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-19648 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr19:41832840-41835360 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs75621460chr1941833784hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXH1MA0479.1chr19:41833281-41833292CCGAATCCACA+6.02
KLF4MA0039.3chr19:41834029-41834040GGAGGGTGTGG-6.32
KLF5MA0599.1chr19:41833549-41833559GGGGCGGGGC-6.02
SPICMA0687.1chr19:41834976-41834990AGAAAGAGGAAGCA+6.04
ZEB1MA0103.3chr19:41833774-41833785GGGCAGGTGGG-6.14
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_01266chr19:41832850-41835062Adrenal_Gland
SE_01941chr19:41826114-41834937Aorta
SE_02341chr19:41827299-41835217Astrocytes
SE_06609chr19:41827940-41835020Brain_Hippocampus_Middle
SE_10534chr19:41829088-41835289CD19_Primary
SE_10928chr19:41826548-41839191CD20
SE_13335chr19:41832811-41834898CD34_Primary_RO01536
SE_14053chr19:41832911-41833520CD34_Primary_RO01549
SE_14717chr19:41828274-41835424CD4_Memory_Primary_7pool
SE_17526chr19:41828356-41835571CD4p_CD25-_CD45RAp_Naive
SE_18470chr19:41831462-41835430CD4p_CD25-_Il17-_PMAstim_Th
SE_19170chr19:41831258-41835426CD4p_CD25-_Il17p_PMAstim_Th17
SE_20013chr19:41827344-41835576CD56
SE_20919chr19:41832350-41835435CD8_Memory_7pool
SE_22408chr19:41828648-41835382CD8_primiary
SE_26210chr19:41832721-41833701Duodenum_Smooth_Muscle
SE_27131chr19:41832876-41835375Esophagus
SE_29782chr19:41832691-41835131Fetal_Muscle
SE_31885chr19:41832910-41835349Gastric
SE_37091chr19:41826651-41835398HSMMtube
SE_38093chr19:41826925-41835502HUVEC
SE_40475chr19:41833510-41834578K562
SE_40475chr19:41834586-41835198K562
SE_41125chr19:41824878-41835177Left_Ventricle
SE_44313chr19:41826974-41833634NHDF-Ad
SE_44313chr19:41833706-41835039NHDF-Ad
SE_44950chr19:41832756-41835161NHLF
SE_45824chr19:41826675-41835471Osteoblasts
SE_48776chr19:41832710-41835338Right_Atrium
SE_50262chr19:41826769-41835431Sigmoid_Colon
SE_52575chr19:41832732-41835420Small_Intestine
SE_62666chr19:41801738-41841748Tonsil
SE_65513chr19:41833044-41835376Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr194183525341835353
chr194183472741835191
Number: 1             
IDChromosomeStartEnd
GH19I041321chr194182700941835422
Enhancer Sequence
ATACACACAC ACTCACTCCC CTCTCCTGGA GAAACACCAT TCCCACAGAT GATTAACATA 60
TGCAGAAAAC ACCACATTTC AAGTCAAACT TACACTTAAA AATGCACAAA TTTACACTCA 120
GAAGAACAGT GAAGATGTTG AGAAAAATAT CAGACACACA ATATGCCCCA GATACATGGC 180
CGACTTGCAG AATCAAACAG TGCCAGAGCA TAAAACCCAC AGAAAATACA ACAGCTTGCC 240
CAGCAGAAAT ACAAAATGCA GACGCACACC CCAGAAATGC AGCGCAGCCA CAAACACACG 300
GAGCTAACAC GTGCTGGGGA CACACATAGA CAAGACCATC CATACCAAAC AGCACACAGG 360
CCCCCAGAAC ACCCATGCCA GACGCAGCTC ACGCCACAAA GCTTGGAATC ACGCACACAA 420
TAAGTTCCTG AACACACAAA TCCGAATCCA CACTGGAACC TCAAATACTC TGCATGTCCA 480
GAGACTAAGG GGGAAGGGGC TTTCTCTCAC CCACCAATCT CCCCACTCCC CCTTGCTGAC 540
CCGGGTCCCA GGCCCGTCTT GGGGGCGGGG GAGGGGGCAG GAAGGCCTGA GCTGGCCTCC 600
CCCAGCAGCT TCCTGCCCCA CGGGGGCTGG ACAGGAAGCT GGGGCTCCAG CCGGAACCCA 660
GGCTCCCCCC ACGACTTCCC TCTGTGGCCC CGGGCCGCCT GCAGAGGCAG GGGCGGGGCA 720
GGGGGAGGAA GCGGGGAGCC CCAAACCCCC TGCCCTGCCC CTGCGGTCGG CCACAGGCGG 780
GGGCAGACTT GTCCCGACGG GGCTGAGCCA CCCATCGGGC CTGGGTGCCA GGGTGGCAGG 840
GCAGGGGCAG TGCGCACGCG GCCAGAGGAA GGTGCTGAGC CCACAGTTTC CCCTCCCCGC 900
CCTGTGGGGC TGTGCCAGCT CAGCCGGCAG CCCTGGGCAG GTGGGCGGGG TGTGTCATGA 960
GGGCGTGTTG GGCAGGCCGA CCACACCGCG AATGTGCAGC CAGCACTTGT CCTCAGGCCG 1020
AGGCACGAGC TGGGGCTGGG CATGTGAGGG CCGCGTCTGC CACCCTGGGG GTGTGTCTGC 1080
TCCGTCTGGG ACCCTGGGTG TGACAGTGTG TCTGGGCGTG ACGTGACGGG GTCGCTGCAA 1140
TCTGTGGGGC CCTGTGGGAC TCCCCAGGCT GGAATTGTGC GTGTGTGGCG GAGGGTGTGG 1200
GATGTCAGAC TGAGTGGGTA AGACCGACCT GCTGTCTGTG AGGTTGTGAC GTGTCAGACC 1260
TCTGTGTGGG GTGTGTCTGG TGGGACTGTG ACAGGTCCGA CTGTGGACAT GCACCCTGGA 1320
CCTGTTTGTG ACTGTGAACC CATGGAGGAG GAGGTGGCTG TTGAGGGATC CATTTCCTGT 1380
CCGGGCTCTG ATGCCGTGAT GCGTGTGCGT GCATGACACT GTTTGAATCA GTGTCTGGTG 1440
TGCGGTGGTT GCGACCATGA CCCTGTGGAA TATATTTGTA TATGACTGTG TTGTGCCAGG 1500
TCCCTATTGA AGTCTCTGCT CGTGTTGTGT CCCAGTGAGG CTCCGAGGCT GGGTGGTGTT 1560
TACGTGATGG GCTGACACTT TCTCTATTTG TATCTGTGTA TATGTGGGCT GCAGCTGCTG 1620
CCAAATGACA CAGCCCATGT GTTACGGGCC CTGCAGGAAT CTCTGTGTGT CCACGGCGGC 1680
TCTGAGAGGT GAATATTTGT GTAGTGTGGG GCACCGTCCG TGTTTCCCGC CGTGTGAGTG 1740
TGTCTGCATG TGTACACGCA CCACATCCTC ATAGGGCTGC AGCGATTACA GCCGAGTCAC 1800
TGTGTCCTAG CTTGTGACTC TGCCTCTTGG GGCCAGACCT CAGCATCTCT ATACCTATCC 1860
ATTTGTTGGC ATGTCCTTGC ATAGTGAACT CCTGCCTCCC CACTCCTCCC TCAGCCCTGT 1920
GTGCTTTGGG ACCTGAGGCC AGAGGAGTAA CCACATTTCT ACCCCTATGC TGAGCTGGGA 1980
GGGCCCCAGG TCCCTGGCAC CCAGACCCAG TGCTGCCAAC AGCTCTCATG CCCACAGGCA 2040
AAGGAACCGC AGCACTCATA CTGTCCTTCC TCCCAGGACA ATCACTGGGT GTGGGGAAGT 2100
GAAACCTAGG AGAAAGAGCA GAAACTGAGA GGCAGGAGAA AGAGGAAGCA GGAGAGAATT 2160
CACAAGCAGG ACCATAGCAG ATGGGAAGAA ATGGAGACAG CAGAGGGAGA CCCACCTGTG 2220
GCTGCTGCCA TTTCTTGCCT GGACAGCTGG TCTGTCTGTG CTCACCCTCA CCCTGACACT 2280
TCTGTCCACT CCCAACCATG AGCAAGACGG CGGACCCTCT GAGCGCCTAG GTCAAACCCT 2340
GCCATGGCTC CTGTCTTCCT TGAGTGCAAG TTCTTTTTTT TTTTTTTTTT GAGATGGAGT 2400
CTCACTCTGT TGCCCAGGCT GGAGTGCAGT GGTGCGACTT TAGCTCACTG CAACCTCTGC 2460
CTCCCCTGTT CATGCGATTC TCCTGCCTCA GGCCCCTGAG TAGCTGGGAT ACAGGTGTGC 2520