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

TagContent
EnhancerAtlas ID
HS073-04657 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr15:67401580-67403720 
Target genes
Number: 1             
NameEnsembl ID
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: 41             
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_48052chr15:67401590-67403339Psoas_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_65752chr15:67401587-67402618Pancreatic_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
CTTTTTGTGT GGAATGCTTG CCATGCACTG AAAAATGCTT TGTGATAGCA GTTTTGAAAA 60
ATTGAGTCAT TTTGCCCTGA TTGAAGCTGG GTGACCTTGT GCAAGTCACT TTAACCCTCT 120
GGGACTTGTG GCCCTCATCT GTAAAATGGG TAGAAGGTCA GAGTGGACCT CGTGGCCTGA 180
GAGGCTAGTA CCCCATGCTG CATGTAAGTC TTACATCCTC CTCTTTGGTG ATTGGATACT 240
GACCCTCTCC CCAGGGGTTC CTGCACAGAG CTGGAATTCT CTCTGGTGTC TTTGCATTCT 300
AGTGGGTGGA ATGCCTTGTT TCTCAGTAGC AATGAGAAAT GTTAATGTGA GGTTATGAAA 360
GCAAGCCAAG AGCCATGGAA TAATTAAAAC ACACACGCAC ACAAAGAAGG AAAAGCGAGA 420
GGGGGAAACA CACTTAATGG ACAAGGGATG AGTAAAACCC AATGGACTGA GAAAACCCCA 480
GAGCTGAACT TCACATGACC CCGCGTGCTG CCTGCAGTTG CGACACCCGC GTGCCCCTTA 540
CGCTCCGCCG GCCTCTCAGT GATGTCAGTG GGCCATGGGC CCCACAGGAA GCAGGGGCTG 600
CCATCAGCCT GGTGGAGCGT GCCAGCCCGC TCCTCCTCCA CGGCCCACTT CCCACCCACC 660
CGGGTCTCCA GATAACATGA AGCCATAGCT CCCAGGCTCG TCAGCGGGGG AAACCAACTC 720
AGTGCTTCTC AGAAAATAGA ACCCCAGCCC ATTAGTGATG TCCACGCAGG CAAGAGATGA 780
CCAAGAAGAA TGTTTGCCTT TTAGGAGTTC TCTGCCTGAA ACCAGCAGGT TTCCTTTAGG 840
GATAGGGTGA CTGTGCTTGC TGAACACCTC TAGGTCGTCA GTGAATGAAA TAATTCATTC 900
TGTGCTTGAG TGTCTAAGAC CCAGGGGGTT TAGGAATAAT TAGGATACTG GCTGTACCCT 960
TGGAGTTCTG TGCTGCTTGG GGGATACGAC TCAAACTCAC AGACATCTGT GGCTCAAATC 1020
AAGGCATATA GATGCAGTGA CTCTTGGAAC ATTCGAGGGA GAATCACCAC CTCTGCTGGT 1080
GGAGGAAAGG CCAGGAACTG CCCACCTAGT TTTCCCATGA CCCCAGCCTG TAGCGGGATA 1140
TGTCAGAAGA TTTGGATTTA GAGGAACTTG GGTTTGACAA AATAGAAGTG TATGTATATA 1200
AACAGAGTTG GGAGTGATGG GGGATAGGAT GCTGACAGCA CCTTGGTAGT CCCTCCCCCT 1260
ACGTGACAGT ATTGACTTCA TAGTGTTGTT GTGAGGCTTG AAGAAGATAC AAGAGGGAAG 1320
AGGAGCGTTC CTTGCCGTGC AGATGCAAAT GCTCATTGTT ACTTGTTCTG CCTCTCTGTG 1380
TCTGTGACAT CCAGCCCTGT GTGGGCTACC CTGGTTGCAA AGTGGGCCTC CTGCCGTTGA 1440
GCAGCTATGG TCCAGTGGGC AGGTACACCA CAGTCATGGA AGCCTAGTTA AATCATTACA 1500
TAATAGTTAG CTCTGTATGA CCAATCTTTT CTTTAAAGAA ATTCTTCCTT TTGGAATAAT 1560
CGTAGATACA CAGAAAAACT GTACACAGAT AATACAGAAA GTTCCAGTGT ACCCCTGACC 1620
CAGATGTCCG TAATGTTAAC ATCTTGTATT ACCATGGTAC ACATGTCAAA ACTCAGAAAC 1680
AACATTGGTA CATTACTAGT AACACAAGTC CAGACTTTAT TCAGTAAACC TTTTGAAAAA 1740
TAATAGCTTT ATTGGCATAT AATTCATACA CCATAAATCT GCTCTTTTAA GGGATATGAT 1800
TTAGTGGTTT TTAGTGTATT AATGGAGTTG TACAACCATC ATCACTATCT AATTTTAGAA 1860
CATTTTCAAC ACCACAAAAA GAAACCTCAT ACCCATTAAC AGTCACTTCC TGCCCATCCC 1920
CCTTAGCCCT GGCAACTTAG TCTACTTTCT GGTTCTCTGG ATTTGCCTCT TTTGGACATT 1980
TCATGTAGAT GAAATCATAC AATTTGTGGA CTTTTGTGTT TGACTTCTTT CACTTAACAT 2040
ATTTTCAGGG TTCATCCATT TGTAGCATGT GTCAGTACTT CATTCCTTTT TATGGCCAAA 2100
TAGTATTCCA GTGTATGGAT ATACCACATT TTGTTTGTCC 2140