EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS154-09963 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr17:76385820-76388550 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs11653383chr1776387103hg19
rs11657987chr1776387363hg19
rs4969178chr1776388202hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MSCMA0665.1chr17:76386414-76386424AACAGCTGTT+6.02
MSCMA0665.1chr17:76386414-76386424AACAGCTGTT-6.02
MYF6MA0667.1chr17:76386414-76386424AACAGCTGTT+6.02
MYF6MA0667.1chr17:76386414-76386424AACAGCTGTT-6.02
Nr2f6(var.2)MA0728.1chr17:76387247-76387262TGAACTACTGACCTC-6.07
Nr2f6(var.2)MA0728.1chr17:76385915-76385930TGAACTCCTGACCTC-6.22
PBX1MA0070.1chr17:76387405-76387417TTTGATTGATTG-6.18
RARAMA0729.1chr17:76387244-76387262TCTTGAACTACTGACCTC-6.1
STAT3MA0144.2chr17:76386545-76386556TTTCTGGGAAG+6.02
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00336chr17:76386145-76387299Adipose_Nuclei
SE_02571chr17:76385876-76387594Astrocytes
SE_02571chr17:76387662-76388894Astrocytes
SE_09402chr17:76385796-76387196CD14
SE_09402chr17:76387807-76389155CD14
SE_29662chr17:76385844-76387171Fetal_Muscle
SE_31461chr17:76385841-76386644Gastric
SE_31461chr17:76386651-76387098Gastric
SE_36965chr17:76385256-76389565HSMMtube
SE_38195chr17:76385655-76388714HUVEC
SE_39141chr17:76385846-76387683IMR90
SE_40802chr17:76385837-76387196Left_Ventricle
SE_42104chr17:76385811-76387176Lung
SE_44143chr17:76385692-76388854NHDF-Ad
SE_44787chr17:76385822-76389178NHLF
SE_45620chr17:76385671-76389091Osteoblasts
SE_50089chr17:76385808-76387604Sigmoid_Colon
SE_51088chr17:76385682-76386847Skeletal_Muscle
SE_51835chr17:76385676-76389059Skeletal_Muscle_Myoblast
SE_52389chr17:76385878-76387198Small_Intestine
SE_53327chr17:76385698-76387613Spleen
SE_55689chr17:76385830-76387298u87
SE_55689chr17:76387543-76388371u87
SE_58926chr17:76309354-76389031Ly3
SE_63627chr17:76385676-76389073HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177638623376387019
chr177638791776388443
Number: 1             
IDChromosomeStartEnd
GH17I078387chr177638364376389156
Enhancer Sequence
AGTAGCTGGG ATTACAGGCA TGTACCACCA CACCCAACTA ATTTTTTTGT GTTTTTAGTA 60
GAGACGGGGT TTCACCATAT TGGCCAGGCT GGTTTTGAAC TCCTGACCTC AAGTTTTCTT 120
CCCGCCTTGG CCTCCCAAAG TGCTAAGATT ATAGGCATGA GCCACTGTGC TGGGCTGCGG 180
CTCTCAGCTT CTTTGAAGGC CGCGTGTGGA CTGACCACAT GACCTGGAGC AGTACAGCGG 240
CACCTGATTT TTGGATGGTC TGAGAGATGG CAGAAATGCT GTGAGGCAGG GGAGACATTG 300
ATTTTATGCT GCTGTTGCCT GTTCCCCCGC CCCCGACCAT GTTTCATTAG TGAATATGAG 360
ACTCTAGGCC CCTTGGGGCC TCGGGTTGAT GGGTTGCTGT GCACCTTTCC CATTGTCCGG 420
TGGTTTCTGC TGCACTGAAG GGTCCTTCGC TCTCCTCTCT TGAGCTTTGC AGGAGGGTGG 480
CCCAGGATTT GGGAAACCCA GGCAGCGAGC CCTGCGTTAC ACATCTAGGC CCTTCATCTG 540
CAAGCTGATG CCTGTGAGTG TCATCACCCC CTCTAGAGAC GGGGGTGGGG GAGGAACAGC 600
TGTTTCCCAC CTCTGCACTG GGTGGCCACG GCCAGTCGCA GACTTCCAGG ATCCACAGAG 660
GCAGCACCTT CTGCTGTTGA CTAAGGTTTT CTTGGCAGTG AATCGGCAGT GACAGACCGG 720
TGGGCTTTCT GGGAAGTGCA GCTGTGGGCC ATCTGTTGTC TGTGCAGGGA CATTTACGAA 780
GCCTGGGAAG ATTGAGGGCT TTATCATGAA GCAAGTGAGT GAAATCATCT TCCTGGAATT 840
TGTGGCCATT CAGGCCTTGG GATGTTTGAG CATCCTCTCC CCCACGTCCC TCTTGAGGTC 900
ACACACTGAA GAGGATTTTC CTGCTGCTGT TTGCAGGACT AGGATTCATA GTAGGTCAGG 960
TCTGTGTGGG GCTCTGGGTG TGCGGTCCCT CCACCCCCAT CTCCCGCAGG TTTTTAGTCA 1020
TTGAGCAGCA GAAATGAAGT TCTGTGGGCA GAAATTCATC TCCTTCAGCC TTGGCCTCAG 1080
TGGAGTGTGG AGTCCGCTGG GGTGCAGCTT TATGTGGTCG AGCTAACACT GGCCAGAAAT 1140
GGTGTGTGAC CCCACCAAAC AGGATGTGTC TGATGGTGAA TGAGTATGGC TCATCATCAC 1200
TCTTTTTTTT TTCTTCTTTG AGATGGAGTC TTGCTCTGTT GCCCAGGCTG GAGTGCAGTG 1260
GCACCATCTC AGCTCACTGC AATCTCCGCC TCCCAGGTTT AAGCGATTCT CCTGCCTCAG 1320
GCTCCTGAGT AGTTGGGATA ACAGGCATCT GCATCATGCC CGGCTAATTT TTTTGTATTT 1380
TTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCTAGG CTTATCTTGA ACTACTGACC 1440
TCAGGTAATC TGCACGCCTC GGCCTCCCAA AGTGGTGGGA TTACAGGCGT GAGCCACCGT 1500
GCGCGGCCAC GGCTCATCAT CACTCTTGAG AGGAGCTCAT TTGCTCCCGT CTCTCCCTGC 1560
TCCAGCTTTT CTTTCCGAGT CTGATTTTGA TTGATTGAGA CAGGGTCTCG CTGTGCCACC 1620
CAGGCTGGAA TGCAATGGCA TGATCATAGC TGGGAGAACA GCCTTGAACT CTTGGGCTCA 1680
GGAGATCCTC CTGCCTCAGC CTCTTGAGTA GCTGGGACTA CAGGTTTGTG CTACCATGCC 1740
CAGGTAACTT TTTTTTGAGA CAGAGTCTCG TTCTGTCACC CAGGCTGGGG TGCAGTGGTG 1800
CGATCTCGCC TCACTGCAAC CTCCACCTCC CTGGTTCAAG CAATTCTCCT GCCTTAGCCT 1860
CCCAAGTAGC TGGGACTACA GTCACATACC ACCACGCCCG GCTAATTTTT GTATTTTTAG 1920
TAGAGAGGGG GTTTCACCAT ATTGGTCAGG CTAGTCTCAA ACACCTGACC TTAGGTTGTC 1980
TACCTGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCCACTGC ACCCAGCCTG 2040
CCCAGCTAAT TTTAAACAAT TTTTTGTAGA CACTGGGTCC TGCTATATTG CTCAGGCTGG 2100
TCCTGAGCTC CTTGACTCAA GCATTCGTCC TGCCTTGGCC TCCCAAAGTG CTAGGATTAT 2160
AGGCCTGAGC CACCATGCTC GGCATAAATT GGATTTTTAA AGAGAAAAGT TTCTTTTTCT 2220
GGGTGCTTCC TTGAATAGAA ATCTTGTTTA TCTCATGAGT CATAAAGCGG GGCATCTGGG 2280
CTGTAATCAT CAGACTTCTG CCAGACTTAC CCTTCTGCTA GGTGTCTTTT AGTGGTGGCT 2340
GCAGGCAAAT ATTTTTGAGG TAGATTCATT AGAACGTTGC CATGTGGTAG CTAACCATGT 2400
GGTAGCTTTT ATGAGTTTAC TTGTGGATGC TCTAAATTTG GTTCCTGAGT TGTTTGGAAT 2460
TAAAGTTTGG GATTTATCTA TAGGTATTGA CACTTCTCAA GTTGCTCAGT TAGTAGGCTC 2520
TTTAAGGAAT AAGAGGAAAG GGGGCTGAAG GAAAAATCCT TTAGCAGAGC TTGAGTTGGG 2580
CTCACTTTTT AAAATGTTCT AGAAAATCTG ACATTCATAA CACAAGCAAC GCACCCATCT 2640
CCCAGCCCCT CTTCACTCCC CAGTAACTGA GGGGGGCTTC TGCAGAAGTA TTTGAGGTAT 2700
TTGAGGTGTG ACCCAGTTGC ATATTTCTTT 2730