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

TagContent
EnhancerAtlas ID
HS138-03901 
Organism
Homo sapiens 
Tissue/cell
MSC_BM 
Coordinate
chr1:235146750-235150030 
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
ATTCAACAAT AACTCCCCAC GTCCCATTCC CCTCAACTAT ATCTTTTTAA AGTGCTTTTC 60
CCAGTGAAGT TTCTAACATT GCTAAAGAAC ATAAAATATA AAAACATGGC CATGCAGCAG 120
GGGCTTTTTA CCCTGCAGAA TGCCCACTAA ACCGTTTCTG TATGTTTAAT TTTTTTAACC 180
AAGGAAGTAG GGGATGCCCA AGATTTGGTC CCCAAACCAG AAAGACTGTG GGTTCCTTGC 240
ATCAAGCCGG GGCTTTTAGT CAACTCTCCC ATGGGGACTC TGTTGGCCCG CTCCACCTCG 300
GGTGTTCCCC CGCCCCTGCC TTTTCCTCTC TCACCTCCCC CATCCACCCC TCTCAGCCTT 360
GCAGTCGACC TGCCTCTCCT CTGGTTGCTC CGTTTGTAGG GAGGGTCTGC TTGAAGGGAG 420
TTCCCATTCT CTCTCACCCA GAGTCAAGGC TCTTGACTCT ATTGTACCTA AAAAGCTCCT 480
GAGGAATTTG ACAAGGCCCC ACCCTCAGAG ATATGGGGTG AAGCCCAGGA ATCTGTATTT 540
TTAACAAGCA TCCCAGGTGA TCCTGATACT TGCACACACC CCCACACACA CCCACGCCGA 600
CTACCCACAC ACTTCCATGG CCCAGAAGTC TGCAGGACCC ACAGCAGGTA TTCGGGACTA 660
TTTGTTCAAT CCACACCTGA GTCGTTGCAC GATTATGCTC AAGTCCCTCG GAACACCTCG 720
CCTGCCATCT GACAGCTTCC CATCCAGAAA CCACACAGTA CAGTAAAAAA CAGAAAAAAG 780
AAAGCCGTTA GACCCCAGTG AATGTTATTT TTAATGAAAG TGGTGCATTT TGACTCACAA 840
TGTTGAAACC AGATTATAAA TGAGTCATCA GTGAATCGAC CACAAAGAGC CTTTGCGGAG 900
GTGATTTACA GGAGAGCTCT GATGTCTGCT GTCCCCTGCA CACGCTTCAC AGAGATGCTG 960
TCAGACGCAG AGCTGGTCTG GGGCATCTGT TGCCGCGTCA GCTCAAAAGG ATGCTGTGTT 1020
GTCACCAATG GGATTCCCCA GCCCAGGCGG TGTTGCGGTC CCACCCACAC AAGGAAGGCG 1080
GCCATCACTG AATAATGCTT GTGGTTACAT CATCATTGCT GGTTTCCAGG TAGTGACTAG 1140
CAGATACTGG AGAGAGACAG GCCATCTGCT CTTCCTGTGC GCCTCAGCTC CTCCCTCATA 1200
CCCACATCCT CTCGCCTGGT CTTCTAGAAG CAGCCCCTAT GCAGACAGAC CAGCAGGACT 1260
GAAAGCTGGA CAGACTCGAG CCGGAGAGCC AGGTGGAACA ACCTGGCCAG AAAGAGTCTG 1320
GCCGCAAAGA GTCTGGCCAC AGCCCCACTT TCCTCATCTC TAAAATGTCC ACATGGCTGC 1380
CTGCCCTGCC CGGCTCAAGG GAATGTTGCA AGGCTCTCAT GGAAACCATG CTTGTGAGGG 1440
TTTTGAGGAC TATCATAGCC CGTCCCAAGG TCAGAGGACA GTAGAAAACA AAAAACTTGC 1500
TTTCAGAGGG TGCTTTCACC AGTCAGCAGC CTCTGCCCCG GGCAAAGCCA GACAACTAAA 1560
ACGGAATGAA TCCGCAGAGT AGGGTGGGGA TGAAATTCTC CACCTCCAAC CCAGAAAGGA 1620
AACGCCAATG CTCATGTTTC CCCTTAGAGA AACAGGCAAT GTTTGAACAG GAACAACGAC 1680
GCCAGAGGGT CAATCCACAC ACAGAACACT CCATCTCCAT GCCGATGGGG GACTGACTGT 1740
CCTGCTGCTG AACTGCACCC CTGGGGCTCT CCAGGACACT CCACTGGTGG CCACACTCAG 1800
GAAAATAAAG AAAAACCTTC AAAAGGACCC TTCTGGCCAT TCAGAGAATG CACAGGCCTG 1860
CTAGCTCCTG CTTGCCTGCT CAGAGCTGCC TCCACTGGGG CAGGAATCTG CAGCCAAGAA 1920
AATCCCTGAC AACCCCAGGG ACAGAAGGGT CAGTCTGGGG GACCATCGAC CAACCCAGCA 1980
ACCCAGATTA GACTGCTCCA CCAGGAACTC TGTGTCCAGA GAGCAGGATC TGCCACAAGC 2040
AAAACTAGGC CTCATTTACT ATTCCACAAT AGCAACTAGA AAGCATGTGA CCCAGAAAAC 2100
CTTCAAAGAA GGCCAGAAAT TCATTAAATC TGAAAAGAAG GGAAGAAGGG CGGGGGAGAG 2160
GAAAACACTG CTTAGCAAAG CCAACTGAAT CCCTCTTCCA TACATCACAG ATGCAGGACC 2220
AGTCTCAGCA TTCAAGAGGA AGAGAAAAAT GAAAACAAAA ACCAATCTGG AGTTGAATGT 2280
CAGCCTTCCC CTCACTGGTT CTGGGTCCTT TGGAAGGCCA TATTGTCCCC GGACCTCTCT 2340
TGCTTCAGTG GCCTTCCTGC CAGGATTGCC ATAAGGATTA AATGGACTCA TATATGTGTT 2400
GTACCTATAC AGTACCTGCA ACACAGTAAA TATCCAATAA ATGTTGGTTT CTTGCTACAA 2460
GAAATTGTAA AATATGGGCA CAAATTCCTC CTACTTTGTT AAGCACATCC CTTGGCAATG 2520
ACTTAGCTGC TACTCCCATC AAGAGTTGTG GTCTATGTCC CTACCCCTTG AATCTGGGCT 2580
AGCCTGGGAC TTGCCTCAAC CAGTAGAATT TAACAAAAGT TACAGTGTGT GACTTCCAAG 2640
GCTAGCCCTT GCCGCTTCCA CTTTTGCCCT CTTGGAATGT GGCCCAGAGA CAACCATCTA 2700
AGGAAGCTGA TCTAGGCCAC TGGAAGAGGG GTGGGCAGAT GGAGAAGTGA TGTCCCCCAA 2760
CCAGCTGCCA GTCACATGAG AGAGGCCATC TCAGATCTTC CGGCCCAGCT GAGCATTCAA 2820
CTAAATGCAG TCACATTAGT GAGCCCAAGC AAAACCGGCA GAACTGTCCA GACAACTCAT 2880
AAAATCAGGA AAACAATCAA TTCTTGTTTT TTTTGTTTGT GTTTTGAGAT GGAGTCTCTG 2940
TTGTAAGGCT GGAGTACAGT GGTGCTGTCT TGGCTCACTG CAACCTCTGC CTCCTGGGCT 3000
CAAGCGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC TACAGGTGCC CGCCACCACG 3060
CTCGGCTAAT TTTTTATATT TTTAGTAGAG ATGGGGTTTC ATCATGTTGG CAAGTATGGT 3120
CTCAATCGCT TGACCTCGTG ATCCACCCAC CTCGGCCTCC CAAAGTGCTG GGATTGCATT 3180
GTTGTTTTAA GTCACTAAGA CTTGCGATGA TTTAGTATGC AGCAAATTCT TACTGAAATA 3240
ACTTTCTTAT TTCCACCTCT AAAACATCTT CTCCCTTGGG 3280