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

TagContent
EnhancerAtlas ID
HS131-00872 
Organism
Homo sapiens 
Tissue/cell
ME-1 
Coordinate
chr1:235146990-235149540 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs57941271chr1235149261hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr1:235147328-235147348CCCCCACACACACCCACGCC+6.07
ZNF263MA0528.1chr1:235147070-235147091TTTTCCTCTCTCACCTCCCCC-6.41
ZNF263MA0528.1chr1:235148891-235148912GAAGAAGGGCGGGGGAGAGGA+6.65
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_02305chr1:235147035-235148901Astrocytes
SE_06052chr1:235147258-235149727Brain_Hippocampus_Middle
SE_25800chr1:235146945-235149402Duodenum_Smooth_Muscle
SE_26806chr1:235147079-235148893Esophagus
SE_29689chr1:235147728-235149217Fetal_Muscle
SE_31235chr1:235146510-235149391Fetal_Thymus
SE_32614chr1:235140175-235154143GM12878
SE_33758chr1:235147075-235148879HCC1954
SE_34767chr1:235147005-235148891HeLa
SE_36058chr1:235146614-235149471HMEC
SE_36952chr1:235146938-235152568HSMMtube
SE_37966chr1:235146872-235149155HUVEC
SE_40653chr1:235147027-235149414Left_Ventricle
SE_42265chr1:235147105-235148992Lung
SE_44202chr1:235146927-235148930NHDF-Ad
SE_45558chr1:235146593-235149758Osteoblasts
SE_47119chr1:235148155-235149767Panc1
SE_50071chr1:235146899-235149198Sigmoid_Colon
SE_51271chr1:235147542-235149156Skeletal_Muscle
SE_52352chr1:235147001-235149055Small_Intestine
SE_53330chr1:235146848-235149167Spleen
SE_56068chr1:235146597-235149251u87
SE_57395chr1:235146972-235147669VACO_503
SE_59274chr1:235138265-235187641Ly3
SE_60969chr1:235059965-235155853HBL1
SE_62329chr1:235047040-235185428Tonsil
SE_63542chr1:235146861-235147654HSMM
SE_63542chr1:235147688-235148831HSMM
SE_65393chr1:235146807-235149156Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1235148474235149499
Number: 1             
IDChromosomeStartEnd
GH01I235010chr1235145789235150146
Enhancer Sequence
ATCAAGCCGG GGCTTTTAGT CAACTCTCCC ATGGGGACTC TGTTGGCCCG CTCCACCTCG 60
GGTGTTCCCC CGCCCCTGCC TTTTCCTCTC TCACCTCCCC CATCCACCCC TCTCAGCCTT 120
GCAGTCGACC TGCCTCTCCT CTGGTTGCTC CGTTTGTAGG GAGGGTCTGC TTGAAGGGAG 180
TTCCCATTCT CTCTCACCCA GAGTCAAGGC TCTTGACTCT ATTGTACCTA AAAAGCTCCT 240
GAGGAATTTG ACAAGGCCCC ACCCTCAGAG ATATGGGGTG AAGCCCAGGA ATCTGTATTT 300
TTAACAAGCA TCCCAGGTGA TCCTGATACT TGCACACACC CCCACACACA CCCACGCCGA 360
CTACCCACAC ACTTCCATGG CCCAGAAGTC TGCAGGACCC ACAGCAGGTA TTCGGGACTA 420
TTTGTTCAAT CCACACCTGA GTCGTTGCAC GATTATGCTC AAGTCCCTCG GAACACCTCG 480
CCTGCCATCT GACAGCTTCC CATCCAGAAA CCACACAGTA CAGTAAAAAA CAGAAAAAAG 540
AAAGCCGTTA GACCCCAGTG AATGTTATTT TTAATGAAAG TGGTGCATTT TGACTCACAA 600
TGTTGAAACC AGATTATAAA TGAGTCATCA GTGAATCGAC CACAAAGAGC CTTTGCGGAG 660
GTGATTTACA GGAGAGCTCT GATGTCTGCT GTCCCCTGCA CACGCTTCAC AGAGATGCTG 720
TCAGACGCAG AGCTGGTCTG GGGCATCTGT TGCCGCGTCA GCTCAAAAGG ATGCTGTGTT 780
GTCACCAATG GGATTCCCCA GCCCAGGCGG TGTTGCGGTC CCACCCACAC AAGGAAGGCG 840
GCCATCACTG AATAATGCTT GTGGTTACAT CATCATTGCT GGTTTCCAGG TAGTGACTAG 900
CAGATACTGG AGAGAGACAG GCCATCTGCT CTTCCTGTGC GCCTCAGCTC CTCCCTCATA 960
CCCACATCCT CTCGCCTGGT CTTCTAGAAG CAGCCCCTAT GCAGACAGAC CAGCAGGACT 1020
GAAAGCTGGA CAGACTCGAG CCGGAGAGCC AGGTGGAACA ACCTGGCCAG AAAGAGTCTG 1080
GCCGCAAAGA GTCTGGCCAC AGCCCCACTT TCCTCATCTC TAAAATGTCC ACATGGCTGC 1140
CTGCCCTGCC CGGCTCAAGG GAATGTTGCA AGGCTCTCAT GGAAACCATG CTTGTGAGGG 1200
TTTTGAGGAC TATCATAGCC CGTCCCAAGG TCAGAGGACA GTAGAAAACA AAAAACTTGC 1260
TTTCAGAGGG TGCTTTCACC AGTCAGCAGC CTCTGCCCCG GGCAAAGCCA GACAACTAAA 1320
ACGGAATGAA TCCGCAGAGT AGGGTGGGGA TGAAATTCTC CACCTCCAAC CCAGAAAGGA 1380
AACGCCAATG CTCATGTTTC CCCTTAGAGA AACAGGCAAT GTTTGAACAG GAACAACGAC 1440
GCCAGAGGGT CAATCCACAC ACAGAACACT CCATCTCCAT GCCGATGGGG GACTGACTGT 1500
CCTGCTGCTG AACTGCACCC CTGGGGCTCT CCAGGACACT CCACTGGTGG CCACACTCAG 1560
GAAAATAAAG AAAAACCTTC AAAAGGACCC TTCTGGCCAT TCAGAGAATG CACAGGCCTG 1620
CTAGCTCCTG CTTGCCTGCT CAGAGCTGCC TCCACTGGGG CAGGAATCTG CAGCCAAGAA 1680
AATCCCTGAC AACCCCAGGG ACAGAAGGGT CAGTCTGGGG GACCATCGAC CAACCCAGCA 1740
ACCCAGATTA GACTGCTCCA CCAGGAACTC TGTGTCCAGA GAGCAGGATC TGCCACAAGC 1800
AAAACTAGGC CTCATTTACT ATTCCACAAT AGCAACTAGA AAGCATGTGA CCCAGAAAAC 1860
CTTCAAAGAA GGCCAGAAAT TCATTAAATC TGAAAAGAAG GGAAGAAGGG CGGGGGAGAG 1920
GAAAACACTG CTTAGCAAAG CCAACTGAAT CCCTCTTCCA TACATCACAG ATGCAGGACC 1980
AGTCTCAGCA TTCAAGAGGA AGAGAAAAAT GAAAACAAAA ACCAATCTGG AGTTGAATGT 2040
CAGCCTTCCC CTCACTGGTT CTGGGTCCTT TGGAAGGCCA TATTGTCCCC GGACCTCTCT 2100
TGCTTCAGTG GCCTTCCTGC CAGGATTGCC ATAAGGATTA AATGGACTCA TATATGTGTT 2160
GTACCTATAC AGTACCTGCA ACACAGTAAA TATCCAATAA ATGTTGGTTT CTTGCTACAA 2220
GAAATTGTAA AATATGGGCA CAAATTCCTC CTACTTTGTT AAGCACATCC CTTGGCAATG 2280
ACTTAGCTGC TACTCCCATC AAGAGTTGTG GTCTATGTCC CTACCCCTTG AATCTGGGCT 2340
AGCCTGGGAC TTGCCTCAAC CAGTAGAATT TAACAAAAGT TACAGTGTGT GACTTCCAAG 2400
GCTAGCCCTT GCCGCTTCCA CTTTTGCCCT CTTGGAATGT GGCCCAGAGA CAACCATCTA 2460
AGGAAGCTGA TCTAGGCCAC TGGAAGAGGG GTGGGCAGAT GGAGAAGTGA TGTCCCCCAA 2520
CCAGCTGCCA GTCACATGAG AGAGGCCATC 2550