EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS109-11376 
Organism
Homo sapiens 
Tissue/cell
Kasumi-1 
Coordinate
chr19:41832760-41835310 
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: 1             
ChromosomeStartEnd
chr194183472741835191
Number: 1             
IDChromosomeStartEnd
GH19I041321chr194182700941835422
Enhancer Sequence
GGAGGCGGAG CTTGCAGTGA GACAAGATCG CGCCATTGCA CTCCAGCCCA GGCGACAGAG 60
CAAGACCCCG TCTTACACAT ATACACACAC ACTCACTCCC CTCTCCTGGA GAAACACCAT 120
TCCCACAGAT GATTAACATA TGCAGAAAAC ACCACATTTC AAGTCAAACT TACACTTAAA 180
AATGCACAAA TTTACACTCA GAAGAACAGT GAAGATGTTG AGAAAAATAT CAGACACACA 240
ATATGCCCCA GATACATGGC CGACTTGCAG AATCAAACAG TGCCAGAGCA TAAAACCCAC 300
AGAAAATACA ACAGCTTGCC CAGCAGAAAT ACAAAATGCA GACGCACACC CCAGAAATGC 360
AGCGCAGCCA CAAACACACG GAGCTAACAC GTGCTGGGGA CACACATAGA CAAGACCATC 420
CATACCAAAC AGCACACAGG CCCCCAGAAC ACCCATGCCA GACGCAGCTC ACGCCACAAA 480
GCTTGGAATC ACGCACACAA TAAGTTCCTG AACACACAAA TCCGAATCCA CACTGGAACC 540
TCAAATACTC TGCATGTCCA GAGACTAAGG GGGAAGGGGC TTTCTCTCAC CCACCAATCT 600
CCCCACTCCC CCTTGCTGAC CCGGGTCCCA GGCCCGTCTT GGGGGCGGGG GAGGGGGCAG 660
GAAGGCCTGA GCTGGCCTCC CCCAGCAGCT TCCTGCCCCA CGGGGGCTGG ACAGGAAGCT 720
GGGGCTCCAG CCGGAACCCA GGCTCCCCCC ACGACTTCCC TCTGTGGCCC CGGGCCGCCT 780
GCAGAGGCAG GGGCGGGGCA GGGGGAGGAA GCGGGGAGCC CCAAACCCCC TGCCCTGCCC 840
CTGCGGTCGG CCACAGGCGG GGGCAGACTT GTCCCGACGG GGCTGAGCCA CCCATCGGGC 900
CTGGGTGCCA GGGTGGCAGG GCAGGGGCAG TGCGCACGCG GCCAGAGGAA GGTGCTGAGC 960
CCACAGTTTC CCCTCCCCGC CCTGTGGGGC TGTGCCAGCT CAGCCGGCAG CCCTGGGCAG 1020
GTGGGCGGGG TGTGTCATGA GGGCGTGTTG GGCAGGCCGA CCACACCGCG AATGTGCAGC 1080
CAGCACTTGT CCTCAGGCCG AGGCACGAGC TGGGGCTGGG CATGTGAGGG CCGCGTCTGC 1140
CACCCTGGGG GTGTGTCTGC TCCGTCTGGG ACCCTGGGTG TGACAGTGTG TCTGGGCGTG 1200
ACGTGACGGG GTCGCTGCAA TCTGTGGGGC CCTGTGGGAC TCCCCAGGCT GGAATTGTGC 1260
GTGTGTGGCG GAGGGTGTGG GATGTCAGAC TGAGTGGGTA AGACCGACCT GCTGTCTGTG 1320
AGGTTGTGAC GTGTCAGACC TCTGTGTGGG GTGTGTCTGG TGGGACTGTG ACAGGTCCGA 1380
CTGTGGACAT GCACCCTGGA CCTGTTTGTG ACTGTGAACC CATGGAGGAG GAGGTGGCTG 1440
TTGAGGGATC CATTTCCTGT CCGGGCTCTG ATGCCGTGAT GCGTGTGCGT GCATGACACT 1500
GTTTGAATCA GTGTCTGGTG TGCGGTGGTT GCGACCATGA CCCTGTGGAA TATATTTGTA 1560
TATGACTGTG TTGTGCCAGG TCCCTATTGA AGTCTCTGCT CGTGTTGTGT CCCAGTGAGG 1620
CTCCGAGGCT GGGTGGTGTT TACGTGATGG GCTGACACTT TCTCTATTTG TATCTGTGTA 1680
TATGTGGGCT GCAGCTGCTG CCAAATGACA CAGCCCATGT GTTACGGGCC CTGCAGGAAT 1740
CTCTGTGTGT CCACGGCGGC TCTGAGAGGT GAATATTTGT GTAGTGTGGG GCACCGTCCG 1800
TGTTTCCCGC CGTGTGAGTG TGTCTGCATG TGTACACGCA CCACATCCTC ATAGGGCTGC 1860
AGCGATTACA GCCGAGTCAC TGTGTCCTAG CTTGTGACTC TGCCTCTTGG GGCCAGACCT 1920
CAGCATCTCT ATACCTATCC ATTTGTTGGC ATGTCCTTGC ATAGTGAACT CCTGCCTCCC 1980
CACTCCTCCC TCAGCCCTGT GTGCTTTGGG ACCTGAGGCC AGAGGAGTAA CCACATTTCT 2040
ACCCCTATGC TGAGCTGGGA GGGCCCCAGG TCCCTGGCAC CCAGACCCAG TGCTGCCAAC 2100
AGCTCTCATG CCCACAGGCA AAGGAACCGC AGCACTCATA CTGTCCTTCC TCCCAGGACA 2160
ATCACTGGGT GTGGGGAAGT GAAACCTAGG AGAAAGAGCA GAAACTGAGA GGCAGGAGAA 2220
AGAGGAAGCA GGAGAGAATT CACAAGCAGG ACCATAGCAG ATGGGAAGAA ATGGAGACAG 2280
CAGAGGGAGA CCCACCTGTG GCTGCTGCCA TTTCTTGCCT GGACAGCTGG TCTGTCTGTG 2340
CTCACCCTCA CCCTGACACT TCTGTCCACT CCCAACCATG AGCAAGACGG CGGACCCTCT 2400
GAGCGCCTAG GTCAAACCCT GCCATGGCTC CTGTCTTCCT TGAGTGCAAG TTCTTTTTTT 2460
TTTTTTTTTT GAGATGGAGT CTCACTCTGT TGCCCAGGCT GGAGTGCAGT GGTGCGACTT 2520
TAGCTCACTG CAACCTCTGC CTCCCCTGTT 2550