EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-03272 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr1:235146580-235149730 
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: 2             
ChromosomeStartEnd
chr1235146978235147112
chr1235148474235149499
Number: 1             
IDChromosomeStartEnd
GH01I235010chr1235145789235150146
Enhancer Sequence
CGCCACCCAA AGTGCTGGGA TTACACGTGT CAGCCACCGT GCCTGGCCTC CATCGTAACC 60
ATTTTTAAGC ACGTTGTTCA GTGGTGTGAC ATGCATTCCC ACTGCTATAC AGCCATCGCC 120
GCTAACCATC TCCAGGCACT TTCATCTTGT AAAATTGAAA CTCTGCACCC ATTCAACAAT 180
AACTCCCCAC GTCCCATTCC CCTCAACTAT ATCTTTTTAA AGTGCTTTTC CCAGTGAAGT 240
TTCTAACATT GCTAAAGAAC ATAAAATATA AAAACATGGC CATGCAGCAG GGGCTTTTTA 300
CCCTGCAGAA TGCCCACTAA ACCGTTTCTG TATGTTTAAT TTTTTTAACC AAGGAAGTAG 360
GGGATGCCCA AGATTTGGTC CCCAAACCAG AAAGACTGTG GGTTCCTTGC ATCAAGCCGG 420
GGCTTTTAGT CAACTCTCCC ATGGGGACTC TGTTGGCCCG CTCCACCTCG GGTGTTCCCC 480
CGCCCCTGCC TTTTCCTCTC TCACCTCCCC CATCCACCCC TCTCAGCCTT GCAGTCGACC 540
TGCCTCTCCT CTGGTTGCTC CGTTTGTAGG GAGGGTCTGC TTGAAGGGAG TTCCCATTCT 600
CTCTCACCCA GAGTCAAGGC TCTTGACTCT ATTGTACCTA AAAAGCTCCT GAGGAATTTG 660
ACAAGGCCCC ACCCTCAGAG ATATGGGGTG AAGCCCAGGA ATCTGTATTT TTAACAAGCA 720
TCCCAGGTGA TCCTGATACT TGCACACACC CCCACACACA CCCACGCCGA CTACCCACAC 780
ACTTCCATGG CCCAGAAGTC TGCAGGACCC ACAGCAGGTA TTCGGGACTA TTTGTTCAAT 840
CCACACCTGA GTCGTTGCAC GATTATGCTC AAGTCCCTCG GAACACCTCG CCTGCCATCT 900
GACAGCTTCC CATCCAGAAA CCACACAGTA CAGTAAAAAA CAGAAAAAAG AAAGCCGTTA 960
GACCCCAGTG AATGTTATTT TTAATGAAAG TGGTGCATTT TGACTCACAA TGTTGAAACC 1020
AGATTATAAA TGAGTCATCA GTGAATCGAC CACAAAGAGC CTTTGCGGAG GTGATTTACA 1080
GGAGAGCTCT GATGTCTGCT GTCCCCTGCA CACGCTTCAC AGAGATGCTG TCAGACGCAG 1140
AGCTGGTCTG GGGCATCTGT TGCCGCGTCA GCTCAAAAGG ATGCTGTGTT GTCACCAATG 1200
GGATTCCCCA GCCCAGGCGG TGTTGCGGTC CCACCCACAC AAGGAAGGCG GCCATCACTG 1260
AATAATGCTT GTGGTTACAT CATCATTGCT GGTTTCCAGG TAGTGACTAG CAGATACTGG 1320
AGAGAGACAG GCCATCTGCT CTTCCTGTGC GCCTCAGCTC CTCCCTCATA CCCACATCCT 1380
CTCGCCTGGT CTTCTAGAAG CAGCCCCTAT GCAGACAGAC CAGCAGGACT GAAAGCTGGA 1440
CAGACTCGAG CCGGAGAGCC AGGTGGAACA ACCTGGCCAG AAAGAGTCTG GCCGCAAAGA 1500
GTCTGGCCAC AGCCCCACTT TCCTCATCTC TAAAATGTCC ACATGGCTGC CTGCCCTGCC 1560
CGGCTCAAGG GAATGTTGCA AGGCTCTCAT GGAAACCATG CTTGTGAGGG TTTTGAGGAC 1620
TATCATAGCC CGTCCCAAGG TCAGAGGACA GTAGAAAACA AAAAACTTGC TTTCAGAGGG 1680
TGCTTTCACC AGTCAGCAGC CTCTGCCCCG GGCAAAGCCA GACAACTAAA ACGGAATGAA 1740
TCCGCAGAGT AGGGTGGGGA TGAAATTCTC CACCTCCAAC CCAGAAAGGA AACGCCAATG 1800
CTCATGTTTC CCCTTAGAGA AACAGGCAAT GTTTGAACAG GAACAACGAC GCCAGAGGGT 1860
CAATCCACAC ACAGAACACT CCATCTCCAT GCCGATGGGG GACTGACTGT CCTGCTGCTG 1920
AACTGCACCC CTGGGGCTCT CCAGGACACT CCACTGGTGG CCACACTCAG GAAAATAAAG 1980
AAAAACCTTC AAAAGGACCC TTCTGGCCAT TCAGAGAATG CACAGGCCTG CTAGCTCCTG 2040
CTTGCCTGCT CAGAGCTGCC TCCACTGGGG CAGGAATCTG CAGCCAAGAA AATCCCTGAC 2100
AACCCCAGGG ACAGAAGGGT CAGTCTGGGG GACCATCGAC CAACCCAGCA ACCCAGATTA 2160
GACTGCTCCA CCAGGAACTC TGTGTCCAGA GAGCAGGATC TGCCACAAGC AAAACTAGGC 2220
CTCATTTACT ATTCCACAAT AGCAACTAGA AAGCATGTGA CCCAGAAAAC CTTCAAAGAA 2280
GGCCAGAAAT TCATTAAATC TGAAAAGAAG GGAAGAAGGG CGGGGGAGAG GAAAACACTG 2340
CTTAGCAAAG CCAACTGAAT CCCTCTTCCA TACATCACAG ATGCAGGACC AGTCTCAGCA 2400
TTCAAGAGGA AGAGAAAAAT GAAAACAAAA ACCAATCTGG AGTTGAATGT CAGCCTTCCC 2460
CTCACTGGTT CTGGGTCCTT TGGAAGGCCA TATTGTCCCC GGACCTCTCT TGCTTCAGTG 2520
GCCTTCCTGC CAGGATTGCC ATAAGGATTA AATGGACTCA TATATGTGTT GTACCTATAC 2580
AGTACCTGCA ACACAGTAAA TATCCAATAA ATGTTGGTTT CTTGCTACAA GAAATTGTAA 2640
AATATGGGCA CAAATTCCTC CTACTTTGTT AAGCACATCC CTTGGCAATG ACTTAGCTGC 2700
TACTCCCATC AAGAGTTGTG GTCTATGTCC CTACCCCTTG AATCTGGGCT AGCCTGGGAC 2760
TTGCCTCAAC CAGTAGAATT TAACAAAAGT TACAGTGTGT GACTTCCAAG GCTAGCCCTT 2820
GCCGCTTCCA CTTTTGCCCT CTTGGAATGT GGCCCAGAGA CAACCATCTA AGGAAGCTGA 2880
TCTAGGCCAC TGGAAGAGGG GTGGGCAGAT GGAGAAGTGA TGTCCCCCAA CCAGCTGCCA 2940
GTCACATGAG AGAGGCCATC TCAGATCTTC CGGCCCAGCT GAGCATTCAA CTAAATGCAG 3000
TCACATTAGT GAGCCCAAGC AAAACCGGCA GAACTGTCCA GACAACTCAT AAAATCAGGA 3060
AAACAATCAA TTCTTGTTTT TTTTGTTTGT GTTTTGAGAT GGAGTCTCTG TTGTAAGGCT 3120
GGAGTACAGT GGTGCTGTCT TGGCTCACTG 3150