EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS175-13363 
Organism
Homo sapiens 
Tissue/cell
SK-N-MC 
Coordinate
chr19:41832750-41835090 
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
Number: 1             
IDChromosomeStartEnd
GH19I041321chr194182700941835422
Enhancer Sequence
CTTGAGCCTG GGAGGCGGAG CTTGCAGTGA GACAAGATCG CGCCATTGCA CTCCAGCCCA 60
GGCGACAGAG CAAGACCCCG TCTTACACAT ATACACACAC ACTCACTCCC CTCTCCTGGA 120
GAAACACCAT TCCCACAGAT GATTAACATA TGCAGAAAAC ACCACATTTC AAGTCAAACT 180
TACACTTAAA AATGCACAAA TTTACACTCA GAAGAACAGT GAAGATGTTG AGAAAAATAT 240
CAGACACACA ATATGCCCCA GATACATGGC CGACTTGCAG AATCAAACAG TGCCAGAGCA 300
TAAAACCCAC AGAAAATACA ACAGCTTGCC CAGCAGAAAT ACAAAATGCA GACGCACACC 360
CCAGAAATGC AGCGCAGCCA CAAACACACG GAGCTAACAC GTGCTGGGGA CACACATAGA 420
CAAGACCATC CATACCAAAC AGCACACAGG CCCCCAGAAC ACCCATGCCA GACGCAGCTC 480
ACGCCACAAA GCTTGGAATC ACGCACACAA TAAGTTCCTG AACACACAAA TCCGAATCCA 540
CACTGGAACC TCAAATACTC TGCATGTCCA GAGACTAAGG GGGAAGGGGC TTTCTCTCAC 600
CCACCAATCT CCCCACTCCC CCTTGCTGAC CCGGGTCCCA GGCCCGTCTT GGGGGCGGGG 660
GAGGGGGCAG GAAGGCCTGA GCTGGCCTCC CCCAGCAGCT TCCTGCCCCA CGGGGGCTGG 720
ACAGGAAGCT GGGGCTCCAG CCGGAACCCA GGCTCCCCCC ACGACTTCCC TCTGTGGCCC 780
CGGGCCGCCT GCAGAGGCAG GGGCGGGGCA GGGGGAGGAA GCGGGGAGCC CCAAACCCCC 840
TGCCCTGCCC CTGCGGTCGG CCACAGGCGG GGGCAGACTT GTCCCGACGG GGCTGAGCCA 900
CCCATCGGGC CTGGGTGCCA GGGTGGCAGG GCAGGGGCAG TGCGCACGCG GCCAGAGGAA 960
GGTGCTGAGC CCACAGTTTC CCCTCCCCGC CCTGTGGGGC TGTGCCAGCT CAGCCGGCAG 1020
CCCTGGGCAG GTGGGCGGGG TGTGTCATGA GGGCGTGTTG GGCAGGCCGA CCACACCGCG 1080
AATGTGCAGC CAGCACTTGT CCTCAGGCCG AGGCACGAGC TGGGGCTGGG CATGTGAGGG 1140
CCGCGTCTGC CACCCTGGGG GTGTGTCTGC TCCGTCTGGG ACCCTGGGTG TGACAGTGTG 1200
TCTGGGCGTG ACGTGACGGG GTCGCTGCAA TCTGTGGGGC CCTGTGGGAC TCCCCAGGCT 1260
GGAATTGTGC GTGTGTGGCG GAGGGTGTGG GATGTCAGAC TGAGTGGGTA AGACCGACCT 1320
GCTGTCTGTG AGGTTGTGAC GTGTCAGACC TCTGTGTGGG GTGTGTCTGG TGGGACTGTG 1380
ACAGGTCCGA CTGTGGACAT GCACCCTGGA CCTGTTTGTG ACTGTGAACC CATGGAGGAG 1440
GAGGTGGCTG TTGAGGGATC CATTTCCTGT CCGGGCTCTG ATGCCGTGAT GCGTGTGCGT 1500
GCATGACACT GTTTGAATCA GTGTCTGGTG TGCGGTGGTT GCGACCATGA CCCTGTGGAA 1560
TATATTTGTA TATGACTGTG TTGTGCCAGG TCCCTATTGA AGTCTCTGCT CGTGTTGTGT 1620
CCCAGTGAGG CTCCGAGGCT GGGTGGTGTT TACGTGATGG GCTGACACTT TCTCTATTTG 1680
TATCTGTGTA TATGTGGGCT GCAGCTGCTG CCAAATGACA CAGCCCATGT GTTACGGGCC 1740
CTGCAGGAAT CTCTGTGTGT CCACGGCGGC TCTGAGAGGT GAATATTTGT GTAGTGTGGG 1800
GCACCGTCCG TGTTTCCCGC CGTGTGAGTG TGTCTGCATG TGTACACGCA CCACATCCTC 1860
ATAGGGCTGC AGCGATTACA GCCGAGTCAC TGTGTCCTAG CTTGTGACTC TGCCTCTTGG 1920
GGCCAGACCT CAGCATCTCT ATACCTATCC ATTTGTTGGC ATGTCCTTGC ATAGTGAACT 1980
CCTGCCTCCC CACTCCTCCC TCAGCCCTGT GTGCTTTGGG ACCTGAGGCC AGAGGAGTAA 2040
CCACATTTCT ACCCCTATGC TGAGCTGGGA GGGCCCCAGG TCCCTGGCAC CCAGACCCAG 2100
TGCTGCCAAC AGCTCTCATG CCCACAGGCA AAGGAACCGC AGCACTCATA CTGTCCTTCC 2160
TCCCAGGACA ATCACTGGGT GTGGGGAAGT GAAACCTAGG AGAAAGAGCA GAAACTGAGA 2220
GGCAGGAGAA AGAGGAAGCA GGAGAGAATT CACAAGCAGG ACCATAGCAG ATGGGAAGAA 2280
ATGGAGACAG CAGAGGGAGA CCCACCTGTG GCTGCTGCCA TTTCTTGCCT GGACAGCTGG 2340