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

TagContent
EnhancerAtlas ID
HS010-01620 
Organism
Homo sapiens 
Tissue/cell
B_cell_blood 
Coordinate
chr15:67401290-67403060 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56324967chr1567402824hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RARA(var.2)MA0730.1chr15:67402064-67402081TGAACTTCACATGACCC-6.52
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00035chr15:67395231-67404229Adipose_Nuclei
SE_02258chr15:67396759-67403330Astrocytes
SE_02918chr15:67402075-67402905Bladder
SE_09181chr15:67398545-67404495CD14
SE_10181chr15:67400628-67404147CD19_Primary
SE_10875chr15:67354078-67404812CD20
SE_20091chr15:67401199-67404038CD56
SE_22489chr15:67402236-67403506CD8_primiary
SE_25827chr15:67401615-67403774Duodenum_Smooth_Muscle
SE_26536chr15:67401500-67403148Esophagus
SE_28551chr15:67401928-67402844Fetal_Intestine_Large
SE_31411chr15:67401581-67403215Gastric
SE_32497chr15:67400723-67404092GM12878
SE_34355chr15:67396760-67403263HCT-116
SE_36917chr15:67388423-67404064HSMMtube
SE_37941chr15:67392792-67403744HUVEC
SE_38858chr15:67395316-67403565IMR90
SE_40854chr15:67401796-67403115Left_Ventricle
SE_42172chr15:67401399-67403115Lung
SE_44149chr15:67395980-67403632NHDF-Ad
SE_44749chr15:67392781-67403987NHLF
SE_45534chr15:67371483-67404480Osteoblasts
SE_47100chr15:67357928-67475420Panc1
SE_47566chr15:67401572-67401979Pancreas
SE_47566chr15:67402027-67402496Pancreas
SE_48052chr15:67395267-67401571Psoas_Muscle
SE_48052chr15:67401590-67403339Psoas_Muscle
SE_48704chr15:67401392-67403179Right_Atrium
SE_50064chr15:67392990-67403253Sigmoid_Colon
SE_51081chr15:67400493-67403362Skeletal_Muscle
SE_51719chr15:67396885-67403666Skeletal_Muscle_Myoblast
SE_52344chr15:67394682-67403275Small_Intestine
SE_53518chr15:67401344-67403260Spleen
SE_55686chr15:67396862-67403181u87
SE_58377chr15:67342858-67447290Ly1
SE_59897chr15:67354926-67408793Ly4
SE_60508chr15:67357006-67428179DHL6
SE_61631chr15:67357404-67427415Toledo
SE_62286chr15:67356723-67443338Tonsil
SE_63504chr15:67396698-67403680HSMM
SE_65752chr15:67399108-67401501Pancreatic_islets
SE_65752chr15:67401587-67402618Pancreatic_islets
SE_67502chr15:67396862-67403181u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr156740189167402640
Number: 1             
IDChromosomeStartEnd
GH15I067100chr156739249567404337
Enhancer Sequence
TACACAGATC AAGGCATGTT TGAAATAGGC TTAATTTTCC TCAAGTTGGC TTTTGTCTCA 60
CAATTGAGTT CTTGTTGACG AAGACCAGTT ATTATTCGTC TTCGTGTCTC TGGAGTCTAG 120
CACCTAGCAC GGTGCCTGAT AAAGCATGGT CACTTCACAA ATACTTGTCG AAGAATGCAT 180
GGGATGAATA TGCATTTGGG TATTTTTAAT GCTTGATGAT TAGAACATTC TCATGGCTTG 240
TTAACTTGTA AGACATAATT TTCATTGTAA GTTCTTTGTG TGTGCAAATG CTTTTTGTGT 300
GGAATGCTTG CCATGCACTG AAAAATGCTT TGTGATAGCA GTTTTGAAAA ATTGAGTCAT 360
TTTGCCCTGA TTGAAGCTGG GTGACCTTGT GCAAGTCACT TTAACCCTCT GGGACTTGTG 420
GCCCTCATCT GTAAAATGGG TAGAAGGTCA GAGTGGACCT CGTGGCCTGA GAGGCTAGTA 480
CCCCATGCTG CATGTAAGTC TTACATCCTC CTCTTTGGTG ATTGGATACT GACCCTCTCC 540
CCAGGGGTTC CTGCACAGAG CTGGAATTCT CTCTGGTGTC TTTGCATTCT AGTGGGTGGA 600
ATGCCTTGTT TCTCAGTAGC AATGAGAAAT GTTAATGTGA GGTTATGAAA GCAAGCCAAG 660
AGCCATGGAA TAATTAAAAC ACACACGCAC ACAAAGAAGG AAAAGCGAGA GGGGGAAACA 720
CACTTAATGG ACAAGGGATG AGTAAAACCC AATGGACTGA GAAAACCCCA GAGCTGAACT 780
TCACATGACC CCGCGTGCTG CCTGCAGTTG CGACACCCGC GTGCCCCTTA CGCTCCGCCG 840
GCCTCTCAGT GATGTCAGTG GGCCATGGGC CCCACAGGAA GCAGGGGCTG CCATCAGCCT 900
GGTGGAGCGT GCCAGCCCGC TCCTCCTCCA CGGCCCACTT CCCACCCACC CGGGTCTCCA 960
GATAACATGA AGCCATAGCT CCCAGGCTCG TCAGCGGGGG AAACCAACTC AGTGCTTCTC 1020
AGAAAATAGA ACCCCAGCCC ATTAGTGATG TCCACGCAGG CAAGAGATGA CCAAGAAGAA 1080
TGTTTGCCTT TTAGGAGTTC TCTGCCTGAA ACCAGCAGGT TTCCTTTAGG GATAGGGTGA 1140
CTGTGCTTGC TGAACACCTC TAGGTCGTCA GTGAATGAAA TAATTCATTC TGTGCTTGAG 1200
TGTCTAAGAC CCAGGGGGTT TAGGAATAAT TAGGATACTG GCTGTACCCT TGGAGTTCTG 1260
TGCTGCTTGG GGGATACGAC TCAAACTCAC AGACATCTGT GGCTCAAATC AAGGCATATA 1320
GATGCAGTGA CTCTTGGAAC ATTCGAGGGA GAATCACCAC CTCTGCTGGT GGAGGAAAGG 1380
CCAGGAACTG CCCACCTAGT TTTCCCATGA CCCCAGCCTG TAGCGGGATA TGTCAGAAGA 1440
TTTGGATTTA GAGGAACTTG GGTTTGACAA AATAGAAGTG TATGTATATA AACAGAGTTG 1500
GGAGTGATGG GGGATAGGAT GCTGACAGCA CCTTGGTAGT CCCTCCCCCT ACGTGACAGT 1560
ATTGACTTCA TAGTGTTGTT GTGAGGCTTG AAGAAGATAC AAGAGGGAAG AGGAGCGTTC 1620
CTTGCCGTGC AGATGCAAAT GCTCATTGTT ACTTGTTCTG CCTCTCTGTG TCTGTGACAT 1680
CCAGCCCTGT GTGGGCTACC CTGGTTGCAA AGTGGGCCTC CTGCCGTTGA GCAGCTATGG 1740
TCCAGTGGGC AGGTACACCA CAGTCATGGA 1770