EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS145-11790 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr19:41832830-41835400 
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
TCTTACACAT ATACACACAC ACTCACTCCC CTCTCCTGGA GAAACACCAT TCCCACAGAT 60
GATTAACATA TGCAGAAAAC ACCACATTTC AAGTCAAACT TACACTTAAA AATGCACAAA 120
TTTACACTCA GAAGAACAGT GAAGATGTTG AGAAAAATAT CAGACACACA ATATGCCCCA 180
GATACATGGC CGACTTGCAG AATCAAACAG TGCCAGAGCA TAAAACCCAC AGAAAATACA 240
ACAGCTTGCC CAGCAGAAAT ACAAAATGCA GACGCACACC CCAGAAATGC AGCGCAGCCA 300
CAAACACACG GAGCTAACAC GTGCTGGGGA CACACATAGA CAAGACCATC CATACCAAAC 360
AGCACACAGG CCCCCAGAAC ACCCATGCCA GACGCAGCTC ACGCCACAAA GCTTGGAATC 420
ACGCACACAA TAAGTTCCTG AACACACAAA TCCGAATCCA CACTGGAACC TCAAATACTC 480
TGCATGTCCA GAGACTAAGG GGGAAGGGGC TTTCTCTCAC CCACCAATCT CCCCACTCCC 540
CCTTGCTGAC CCGGGTCCCA GGCCCGTCTT GGGGGCGGGG GAGGGGGCAG GAAGGCCTGA 600
GCTGGCCTCC CCCAGCAGCT TCCTGCCCCA CGGGGGCTGG ACAGGAAGCT GGGGCTCCAG 660
CCGGAACCCA GGCTCCCCCC ACGACTTCCC TCTGTGGCCC CGGGCCGCCT GCAGAGGCAG 720
GGGCGGGGCA GGGGGAGGAA GCGGGGAGCC CCAAACCCCC TGCCCTGCCC CTGCGGTCGG 780
CCACAGGCGG GGGCAGACTT GTCCCGACGG GGCTGAGCCA CCCATCGGGC CTGGGTGCCA 840
GGGTGGCAGG GCAGGGGCAG TGCGCACGCG GCCAGAGGAA GGTGCTGAGC CCACAGTTTC 900
CCCTCCCCGC CCTGTGGGGC TGTGCCAGCT CAGCCGGCAG CCCTGGGCAG GTGGGCGGGG 960
TGTGTCATGA GGGCGTGTTG GGCAGGCCGA CCACACCGCG AATGTGCAGC CAGCACTTGT 1020
CCTCAGGCCG AGGCACGAGC TGGGGCTGGG CATGTGAGGG CCGCGTCTGC CACCCTGGGG 1080
GTGTGTCTGC TCCGTCTGGG ACCCTGGGTG TGACAGTGTG TCTGGGCGTG ACGTGACGGG 1140
GTCGCTGCAA TCTGTGGGGC CCTGTGGGAC TCCCCAGGCT GGAATTGTGC GTGTGTGGCG 1200
GAGGGTGTGG GATGTCAGAC TGAGTGGGTA AGACCGACCT GCTGTCTGTG AGGTTGTGAC 1260
GTGTCAGACC TCTGTGTGGG GTGTGTCTGG TGGGACTGTG ACAGGTCCGA CTGTGGACAT 1320
GCACCCTGGA CCTGTTTGTG ACTGTGAACC CATGGAGGAG GAGGTGGCTG TTGAGGGATC 1380
CATTTCCTGT CCGGGCTCTG ATGCCGTGAT GCGTGTGCGT GCATGACACT GTTTGAATCA 1440
GTGTCTGGTG TGCGGTGGTT GCGACCATGA CCCTGTGGAA TATATTTGTA TATGACTGTG 1500
TTGTGCCAGG TCCCTATTGA AGTCTCTGCT CGTGTTGTGT CCCAGTGAGG CTCCGAGGCT 1560
GGGTGGTGTT TACGTGATGG GCTGACACTT TCTCTATTTG TATCTGTGTA TATGTGGGCT 1620
GCAGCTGCTG CCAAATGACA CAGCCCATGT GTTACGGGCC CTGCAGGAAT CTCTGTGTGT 1680
CCACGGCGGC TCTGAGAGGT GAATATTTGT GTAGTGTGGG GCACCGTCCG TGTTTCCCGC 1740
CGTGTGAGTG TGTCTGCATG TGTACACGCA CCACATCCTC ATAGGGCTGC AGCGATTACA 1800
GCCGAGTCAC TGTGTCCTAG CTTGTGACTC TGCCTCTTGG GGCCAGACCT CAGCATCTCT 1860
ATACCTATCC ATTTGTTGGC ATGTCCTTGC ATAGTGAACT CCTGCCTCCC CACTCCTCCC 1920
TCAGCCCTGT GTGCTTTGGG ACCTGAGGCC AGAGGAGTAA CCACATTTCT ACCCCTATGC 1980
TGAGCTGGGA GGGCCCCAGG TCCCTGGCAC CCAGACCCAG TGCTGCCAAC AGCTCTCATG 2040
CCCACAGGCA AAGGAACCGC AGCACTCATA CTGTCCTTCC TCCCAGGACA ATCACTGGGT 2100
GTGGGGAAGT GAAACCTAGG AGAAAGAGCA GAAACTGAGA GGCAGGAGAA AGAGGAAGCA 2160
GGAGAGAATT CACAAGCAGG ACCATAGCAG ATGGGAAGAA ATGGAGACAG CAGAGGGAGA 2220
CCCACCTGTG GCTGCTGCCA TTTCTTGCCT GGACAGCTGG TCTGTCTGTG CTCACCCTCA 2280
CCCTGACACT TCTGTCCACT CCCAACCATG AGCAAGACGG CGGACCCTCT GAGCGCCTAG 2340
GTCAAACCCT GCCATGGCTC CTGTCTTCCT TGAGTGCAAG TTCTTTTTTT TTTTTTTTTT 2400
GAGATGGAGT CTCACTCTGT TGCCCAGGCT GGAGTGCAGT GGTGCGACTT TAGCTCACTG 2460
CAACCTCTGC CTCCCCTGTT CATGCGATTC TCCTGCCTCA GGCCCCTGAG TAGCTGGGAT 2520
ACAGGTGTGC ACCACAATGC CAGACTAATT TTTTTTTGTA TTTTTTATTT 2570