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

TagContent
EnhancerAtlas ID
HS060-33158 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr8:28198180-28199040 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr8:28198817-28198828GGATGACTCAT+6.62
JUN(var.2)MA0489.1chr8:28198819-28198833ATGACTCATCTCCA-6.11
JUNBMA0490.1chr8:28198817-28198828GGATGACTCAT+6.62
SRFMA0083.3chr8:28198756-28198772TTACCAAATATGGACA-6.11
SRFMA0083.3chr8:28198756-28198772TTACCAAATATGGACA+6.45
ZNF263MA0528.1chr8:28198296-28198317GGGGCAAGAGGGGGAAAAGGG+6.16
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_10187chr8:28193185-28199915CD19_Primary
SE_10881chr8:28188182-28210367CD20
SE_20270chr8:28193633-28199622CD56
SE_27701chr8:28198699-28202802Fetal_Intestine
SE_28577chr8:28197992-28203262Fetal_Intestine_Large
SE_40988chr8:28198227-28199833Left_Ventricle
SE_58992chr8:28165452-28207351Ly3
SE_59946chr8:28164768-28207284Ly4
SE_61002chr8:28174118-28277761HBL1
SE_63042chr8:28186067-28207603Tonsil
SE_65386chr8:28196394-28198883Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr82819830528198911
chr82819868028199000
Enhancer Sequence
CACGTTCTGC AGTCTATACA AGAAGCATGG CACCCGCATC TGCTTCTGGT GAGGCCCTCG 60
GGGAGCTTTT ACTCATGGCA GAAGGCAAGG GGAGCTGGCG TGCCACATGG CAAGAGGGGG 120
CAAGAGGGGG AAAAGGGGAG GTCCCAGCCT CTTTAACAAC CAGATCTCCC ACGAACTCAT 180
TACCATAGGG TGGGCACAAA GGCATTCCTG AAGGATCCAC CCCCATGACC CAAACACCAC 240
CCACTAGGCC CACCTCCAAC ATTAGGGATC ACATCTCAAC ATGAAATTGG AAGAGGACAA 300
ACTTCTAAAC TGTATCATTG TCCTAACACA AAGAACCAGT CAGATCATCA AAATCACCCC 360
AAAACATTAC CCAAGTGGGG CTTTTCCCTG AGTCCGAGCA TAAGAGAAAA ATGTCTGCAT 420
GTGCTATTTT AAGTTGCGTC CCATGTGTCA GAGGTAGCCG TGTCACTAAT AACCTTCCTT 480
GATGATCTAT TAGTACATAT GCTAATGTTT GGTGCCCACA CTTTAGCATG GAGACGGCCC 540
CTTTGCAGGT AGGCCAACAT GTTCACCACG GGCCTGTTAC CAAATATGGA CACGTGTATT 600
AAGTTGTGAA GAGAAAGCTG ATGTGTTTAT TTTAGCAGGA TGACTCATCT CCAAAGGCCC 660
CAAATTAACC TGCACTGCTT TTGAAGTCAT ACTCACTCTT GGATCCTTCA CAAGCCTCCT 720
ATTTCTTTCT AACACATATC TGCACAGCAC CTAACAGTAA ATCGTTCAGA AGTAGCATGG 780
GTTGAATTCT TTCAAATCTT AAAGACATTC TTCTTTAAAG TGGCTCTTCA GGGACACTGA 840
AGCTCATGTC TAATTCTGAA 860