EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-31906 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr5:77800020-77802750 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2277015chr577800588hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CDX2MA0465.1chr5:77800496-77800507TTTTATTGCTT-6.32
NFAT5MA0606.1chr5:77801263-77801273AATGGAAAAT-6.02
NFATC1MA0624.1chr5:77801263-77801273AATGGAAAAT-6.02
NFATC3MA0625.1chr5:77801263-77801273AATGGAAAAT-6.02
RFX5MA0510.2chr5:77802209-77802225TGTTGCTCTGGCAACA+6.07
TFAP2CMA0524.2chr5:77800651-77800663AGCCCCAGGGCA+6.11
ZNF263MA0528.1chr5:77801288-77801309AGGGGAGGGGGAGGAAGGAGC+6.39
ZNF263MA0528.1chr5:77801282-77801303AGGGGAAGGGGAGGGGGAGGA+7.13
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00744chr5:77799632-77801875Adipose_Nuclei
SE_01516chr5:77799767-77800303Adrenal_Gland
SE_01516chr5:77800328-77801493Adrenal_Gland
SE_02084chr5:77799778-77800837Aorta
SE_02084chr5:77800926-77801565Aorta
SE_02699chr5:77799902-77801516Astrocytes
SE_13177chr5:77799978-77800634CD34_Primary_RO01480
SE_13761chr5:77800385-77802849CD34_Primary_RO01536
SE_14327chr5:77801643-77802549CD34_Primary_RO01549
SE_25910chr5:77799563-77808605Duodenum_Smooth_Muscle
SE_29638chr5:77799474-77803204Fetal_Muscle
SE_36101chr5:77799462-77802446HMEC
SE_37067chr5:77799145-77808361HSMMtube
SE_38069chr5:77799675-77802027HUVEC
SE_44285chr5:77799521-77806899NHDF-Ad
SE_44858chr5:77799562-77803016NHLF
SE_45582chr5:77799364-77805037Osteoblasts
SE_51920chr5:77799864-77801500Skeletal_Muscle_Myoblast
SE_53244chr5:77799914-77802051Small_Intestine
SE_54871chr5:77799656-77803259Stomach_Smooth_Muscle
SE_55657chr5:77799733-77802979u87
SE_61959chr5:77778881-77810352Toledo
SE_63730chr5:77799657-77801514HSMM
SE_63730chr5:77801893-77802698HSMM
SE_64735chr5:77799668-77802009NHEK
SE_67593chr5:77799733-77802979u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr57780022577801516
Number: 1             
IDChromosomeStartEnd
GH05I078503chr57779962577808076
Enhancer Sequence
CCTTGTGCTC ACCAGGAACA AAAGGAAGGG CTGTTCCCTC TACTCTCCCC ATGCCTCTTT 60
GAGGGTGTTC TGAAGGTGGG CAACCAAGGT CACACCACCC CAGAGAAAGC CCGGTGACTT 120
TTTCAGGAGA AAAATTCTGA GGCAGGGCTC CATGTGTGCC AGGCATCTCC GTCCATCTCC 180
CTATGCTTCC CAAGCCCCTG TTCTGATTTC TCTCCTCTCA GTGGCTGACC TTGTCTTTTG 240
GGCCTGAGAG TGAATGAGTA GGGCATGAGA TCAGTCATGG GGTTGGGCTA TGGTCATAAC 300
CTTGATGCTT AAGGTGATTT TTTACCCTGT GTAAAAAGCA GTAAGAATAC CAAATCCTGG 360
AGAGTGATCA GCTGCATTTC GTATGCCCAC CCATACTTCC ATGCATCAGA TTTATGACAA 420
AAGCAATTAT ATAAGCAGCA AAGGCAAAAC CCCCACGTGT CTGTCTCTGC TTTTCCTTTT 480
ATTGCTTTTT TTCATGTTGT CCTCTTTCAC CCTCAATCAT TGCTCACTTC CAAGAAGGCT 540
GAGCCTGCAT ACACCAGGCC CTTCACCGCC ACTGCCAGCG CCATTCCCAC GACCACACAC 600
CCTTCACCCC AGCCCTGCAG AGGCAGGGTT CAGCCCCAGG GCAATCTATC TGGTCAGACT 660
GGTGGGGCAG CTTGCTAAGG CTGTCCTGCT GGACTGAGAC CCATGCAGGC AGAGGGCTGG 720
AGGGAGTAGA GTGTGAGAGC CAGCCCAGCA TAAAGGGAAG ACTGGAAGAT AGCAGGCAGC 780
TGGCCGGTGG CTCATGCTTA TGGCAGTCCC TGTGGAATAG GCCCAGCCAG CACAAGTGAG 840
CCAAATCCTG AGCTCAGTTT AATGGCTTCG GTCCCAAACC TGAGTCACTG GGGATTCCAT 900
GGACTTCTAA GAGAGCCCTA CACGCATTTC CAAAAACAAA CTGCTTGATG TTGTCATGGA 960
AAACCTGGAT CTTTGCATTC TATGGTTTCA CGATGGATTA CATCCAGGTC ACAACCTAAG 1020
GAAGACAGCT GGCAAAAAGC CAACCCTGCT GGCTGATCAC CCGGCTTTTG TAATGAATCC 1080
CAGAGGGATG CAAACTGATG TGTGTTGCTG CCTCTGCCAA GTCCTTGGAC AAGTTCTCAC 1140
CTCATGAAGA CTAATCAACC TGTGATTTAC TCCGCCAGGA GAATCTCAGA AGCCACCTGC 1200
AATCAACACT CAACGGCTAG AAGCTGCCTC CAGAAAGAGA AGGAATGGAA AATGTGTGTG 1260
TCAGGGGAAG GGGAGGGGGA GGAAGGAGCT CTGTTTTCTT GTCAATTTGA CTGCTCTCTC 1320
CTGCCTTTTA AAAAAATGAT CTGAGGACAC CCCTGGTTAC ACCAAAGCCA CAGGACTGCT 1380
GTGCACCCTG AGCTCCAACA CAGGCAGGCT CTTAAGGACA GGGAAGGCCC CTACACACTG 1440
TATTTGTGTT TGATTGGAAC AGAGTAAGGT CAATTCTAAA AGCTACAAGA TATCCCTGTT 1500
CCGTAGAATG CAACAAATCC GGGAAACAAA TAATATACTA AAACTTGCCA AGAAAGCAGA 1560
AATACTTTGA TAATGATTCT ATAGCTACCA TTTATTATTT ACTGTGTGTT AAGCACTATG 1620
CTTAAGCCTT TCTCATATAT TATCTAACTT AATCCTCAGA ACAGTCCTGA GGTATAAACC 1680
TATTGTTATG CCCATTTTAC AAGTGAGAAA ACTATGGTTC AGAAAAGTGA GGCAAATTGG 1740
TCCGTGTTTC ACAGGCACAT TCAGGTGAGG CCTGAACCCT CATTACTGAG TGAGTGCTGA 1800
ATGTCAAGGA CATGTGCACA GTATTTAGAA AGTATCAGCC GGGTGTCCAC CTAATGGTGC 1860
CCTGAAGGCA GATCCTGCTA TCTGGATTCA CATAACAGGC AATGATTATA TTTCATTACT 1920
GCTTAAGTTA GCCCAGAGTT TGGGATTTCC ATTGAAGTAG CAGATTCTTT CACACCCAGT 1980
TTCTAAACTC AGAATATCAA GATTTTGATT ATTTATGCTG TGTTTTTTTA TAGACAGTGA 2040
AGGCTACACA AGCCTGTGGC CTATTTATAT CTTAAAATTA GGTGTAGCAA AAGAATATGC 2100
TTACGATCAT TTCTCATCCA GTCACATTTT TGCCAAAATG TAAGTTGTAA GAACAAACAC 2160
AGCCTGAGTG TATTTCTAAA GAATCCTTTT GTTGCTCTGG CAACAGCCTC CTTTCTCACC 2220
ATTTGTTTCA GTGTTGAAGA GATCCAGGGC TGAGGGAGAG GGGGCATAGG GAGAGAAAAG 2280
GCAGATGCTC CCAGCTGCAG CAAGTCCTTG CTGAGGCTGG GGCTGACCAG AGGCTATCAC 2340
AGATTGGCCA ACGGGAGAAA GCAAGCCAGC CCTTTCAGAT GCCAGTATGG CAATGTCCTC 2400
AGCCACAGAT TCAAGAACCA CAGCTGCCCT TTACATTGGC TTGATGTGCA TGATGAGACC 2460
TCCAATAGGG GAGAAAGTGC CCACTGAATC ATGAGAAGGA TAGCTCAGTC CCTCTTTTTT 2520
ATGATTTTTT CTCTGAGGGG TGATGCTAGG CTGGAAGGAG AAAAGAAACC AGTTCTTTCC 2580
TGTATTTCAG CACTTAGTCT TAGATCAGTG GCTCCTAGAC AGCAGTCAAA CTATGCAGGA 2640
ATCTCTGCCT TGTGCCAATT TAAAATTCTG AGTAATTTCA GAATTTTTGA GATGCTGCAT 2700
AAGTAACAGG GGTAGGGAGG AAGTTAAAGC 2730