EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-24491 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr19:41832740-41835340 
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
AGGAGAATCG CTTGAGCCTG GGAGGCGGAG CTTGCAGTGA GACAAGATCG CGCCATTGCA 60
CTCCAGCCCA GGCGACAGAG CAAGACCCCG TCTTACACAT ATACACACAC ACTCACTCCC 120
CTCTCCTGGA GAAACACCAT TCCCACAGAT GATTAACATA TGCAGAAAAC ACCACATTTC 180
AAGTCAAACT TACACTTAAA AATGCACAAA TTTACACTCA GAAGAACAGT GAAGATGTTG 240
AGAAAAATAT CAGACACACA ATATGCCCCA GATACATGGC CGACTTGCAG AATCAAACAG 300
TGCCAGAGCA TAAAACCCAC AGAAAATACA ACAGCTTGCC CAGCAGAAAT ACAAAATGCA 360
GACGCACACC CCAGAAATGC AGCGCAGCCA CAAACACACG GAGCTAACAC GTGCTGGGGA 420
CACACATAGA CAAGACCATC CATACCAAAC AGCACACAGG CCCCCAGAAC ACCCATGCCA 480
GACGCAGCTC ACGCCACAAA GCTTGGAATC ACGCACACAA TAAGTTCCTG AACACACAAA 540
TCCGAATCCA CACTGGAACC TCAAATACTC TGCATGTCCA GAGACTAAGG GGGAAGGGGC 600
TTTCTCTCAC CCACCAATCT CCCCACTCCC CCTTGCTGAC CCGGGTCCCA GGCCCGTCTT 660
GGGGGCGGGG GAGGGGGCAG GAAGGCCTGA GCTGGCCTCC CCCAGCAGCT TCCTGCCCCA 720
CGGGGGCTGG ACAGGAAGCT GGGGCTCCAG CCGGAACCCA GGCTCCCCCC ACGACTTCCC 780
TCTGTGGCCC CGGGCCGCCT GCAGAGGCAG GGGCGGGGCA GGGGGAGGAA GCGGGGAGCC 840
CCAAACCCCC TGCCCTGCCC CTGCGGTCGG CCACAGGCGG GGGCAGACTT GTCCCGACGG 900
GGCTGAGCCA CCCATCGGGC CTGGGTGCCA GGGTGGCAGG GCAGGGGCAG TGCGCACGCG 960
GCCAGAGGAA GGTGCTGAGC CCACAGTTTC CCCTCCCCGC CCTGTGGGGC TGTGCCAGCT 1020
CAGCCGGCAG CCCTGGGCAG GTGGGCGGGG TGTGTCATGA GGGCGTGTTG GGCAGGCCGA 1080
CCACACCGCG AATGTGCAGC CAGCACTTGT CCTCAGGCCG AGGCACGAGC TGGGGCTGGG 1140
CATGTGAGGG CCGCGTCTGC CACCCTGGGG GTGTGTCTGC TCCGTCTGGG ACCCTGGGTG 1200
TGACAGTGTG TCTGGGCGTG ACGTGACGGG GTCGCTGCAA TCTGTGGGGC CCTGTGGGAC 1260
TCCCCAGGCT GGAATTGTGC GTGTGTGGCG GAGGGTGTGG GATGTCAGAC TGAGTGGGTA 1320
AGACCGACCT GCTGTCTGTG AGGTTGTGAC GTGTCAGACC TCTGTGTGGG GTGTGTCTGG 1380
TGGGACTGTG ACAGGTCCGA CTGTGGACAT GCACCCTGGA CCTGTTTGTG ACTGTGAACC 1440
CATGGAGGAG GAGGTGGCTG TTGAGGGATC CATTTCCTGT CCGGGCTCTG ATGCCGTGAT 1500
GCGTGTGCGT GCATGACACT GTTTGAATCA GTGTCTGGTG TGCGGTGGTT GCGACCATGA 1560
CCCTGTGGAA TATATTTGTA TATGACTGTG TTGTGCCAGG TCCCTATTGA AGTCTCTGCT 1620
CGTGTTGTGT CCCAGTGAGG CTCCGAGGCT GGGTGGTGTT TACGTGATGG GCTGACACTT 1680
TCTCTATTTG TATCTGTGTA TATGTGGGCT GCAGCTGCTG CCAAATGACA CAGCCCATGT 1740
GTTACGGGCC CTGCAGGAAT CTCTGTGTGT CCACGGCGGC TCTGAGAGGT GAATATTTGT 1800
GTAGTGTGGG GCACCGTCCG TGTTTCCCGC CGTGTGAGTG TGTCTGCATG TGTACACGCA 1860
CCACATCCTC ATAGGGCTGC AGCGATTACA GCCGAGTCAC TGTGTCCTAG CTTGTGACTC 1920
TGCCTCTTGG GGCCAGACCT CAGCATCTCT ATACCTATCC ATTTGTTGGC ATGTCCTTGC 1980
ATAGTGAACT CCTGCCTCCC CACTCCTCCC TCAGCCCTGT GTGCTTTGGG ACCTGAGGCC 2040
AGAGGAGTAA CCACATTTCT ACCCCTATGC TGAGCTGGGA GGGCCCCAGG TCCCTGGCAC 2100
CCAGACCCAG TGCTGCCAAC AGCTCTCATG CCCACAGGCA AAGGAACCGC AGCACTCATA 2160
CTGTCCTTCC TCCCAGGACA ATCACTGGGT GTGGGGAAGT GAAACCTAGG AGAAAGAGCA 2220
GAAACTGAGA GGCAGGAGAA AGAGGAAGCA GGAGAGAATT CACAAGCAGG ACCATAGCAG 2280
ATGGGAAGAA ATGGAGACAG CAGAGGGAGA CCCACCTGTG GCTGCTGCCA TTTCTTGCCT 2340
GGACAGCTGG TCTGTCTGTG CTCACCCTCA CCCTGACACT TCTGTCCACT CCCAACCATG 2400
AGCAAGACGG CGGACCCTCT GAGCGCCTAG GTCAAACCCT GCCATGGCTC CTGTCTTCCT 2460
TGAGTGCAAG TTCTTTTTTT TTTTTTTTTT GAGATGGAGT CTCACTCTGT TGCCCAGGCT 2520
GGAGTGCAGT GGTGCGACTT TAGCTCACTG CAACCTCTGC CTCCCCTGTT CATGCGATTC 2580
TCCTGCCTCA GGCCCCTGAG 2600