EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-21941 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr5:77799930-77801960 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2277015chr577800588hg19
TF binding sites/motifs
Number: 7             
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
TFAP2CMA0524.2chr5:77800651-77800663AGCCCCAGGGCA+6.11
ZNF263MA0528.1chr5:77801288-77801309AGGGGAGGGGGAGGAAGGAGC+6.39
ZNF263MA0528.1chr5:77801282-77801303AGGGGAAGGGGAGGGGGAGGA+7.13
Number of super-enhancer constituents: 25             
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_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
GAACTGTTGG ACCTGACTTC TGGTGGAGCA TCATCTGTCT GGACAGCCAG AAACCAAGAG 60
CCTCCCTTTG GCAGCCAGAA GTCCTCAGGG CCTTGTGCTC ACCAGGAACA AAAGGAAGGG 120
CTGTTCCCTC TACTCTCCCC ATGCCTCTTT GAGGGTGTTC TGAAGGTGGG CAACCAAGGT 180
CACACCACCC CAGAGAAAGC CCGGTGACTT TTTCAGGAGA AAAATTCTGA GGCAGGGCTC 240
CATGTGTGCC AGGCATCTCC GTCCATCTCC CTATGCTTCC CAAGCCCCTG TTCTGATTTC 300
TCTCCTCTCA GTGGCTGACC TTGTCTTTTG GGCCTGAGAG TGAATGAGTA GGGCATGAGA 360
TCAGTCATGG GGTTGGGCTA TGGTCATAAC CTTGATGCTT AAGGTGATTT TTTACCCTGT 420
GTAAAAAGCA GTAAGAATAC CAAATCCTGG AGAGTGATCA GCTGCATTTC GTATGCCCAC 480
CCATACTTCC ATGCATCAGA TTTATGACAA AAGCAATTAT ATAAGCAGCA AAGGCAAAAC 540
CCCCACGTGT CTGTCTCTGC TTTTCCTTTT ATTGCTTTTT TTCATGTTGT CCTCTTTCAC 600
CCTCAATCAT TGCTCACTTC CAAGAAGGCT GAGCCTGCAT ACACCAGGCC CTTCACCGCC 660
ACTGCCAGCG CCATTCCCAC GACCACACAC CCTTCACCCC AGCCCTGCAG AGGCAGGGTT 720
CAGCCCCAGG GCAATCTATC TGGTCAGACT GGTGGGGCAG CTTGCTAAGG CTGTCCTGCT 780
GGACTGAGAC CCATGCAGGC AGAGGGCTGG AGGGAGTAGA GTGTGAGAGC CAGCCCAGCA 840
TAAAGGGAAG ACTGGAAGAT AGCAGGCAGC TGGCCGGTGG CTCATGCTTA TGGCAGTCCC 900
TGTGGAATAG GCCCAGCCAG CACAAGTGAG CCAAATCCTG AGCTCAGTTT AATGGCTTCG 960
GTCCCAAACC TGAGTCACTG GGGATTCCAT GGACTTCTAA GAGAGCCCTA CACGCATTTC 1020
CAAAAACAAA CTGCTTGATG TTGTCATGGA AAACCTGGAT CTTTGCATTC TATGGTTTCA 1080
CGATGGATTA CATCCAGGTC ACAACCTAAG GAAGACAGCT GGCAAAAAGC CAACCCTGCT 1140
GGCTGATCAC CCGGCTTTTG TAATGAATCC CAGAGGGATG CAAACTGATG TGTGTTGCTG 1200
CCTCTGCCAA GTCCTTGGAC AAGTTCTCAC CTCATGAAGA CTAATCAACC TGTGATTTAC 1260
TCCGCCAGGA GAATCTCAGA AGCCACCTGC AATCAACACT CAACGGCTAG AAGCTGCCTC 1320
CAGAAAGAGA AGGAATGGAA AATGTGTGTG TCAGGGGAAG GGGAGGGGGA GGAAGGAGCT 1380
CTGTTTTCTT GTCAATTTGA CTGCTCTCTC CTGCCTTTTA AAAAAATGAT CTGAGGACAC 1440
CCCTGGTTAC ACCAAAGCCA CAGGACTGCT GTGCACCCTG AGCTCCAACA CAGGCAGGCT 1500
CTTAAGGACA GGGAAGGCCC CTACACACTG TATTTGTGTT TGATTGGAAC AGAGTAAGGT 1560
CAATTCTAAA AGCTACAAGA TATCCCTGTT CCGTAGAATG CAACAAATCC GGGAAACAAA 1620
TAATATACTA AAACTTGCCA AGAAAGCAGA AATACTTTGA TAATGATTCT ATAGCTACCA 1680
TTTATTATTT ACTGTGTGTT AAGCACTATG CTTAAGCCTT TCTCATATAT TATCTAACTT 1740
AATCCTCAGA ACAGTCCTGA GGTATAAACC TATTGTTATG CCCATTTTAC AAGTGAGAAA 1800
ACTATGGTTC AGAAAAGTGA GGCAAATTGG TCCGTGTTTC ACAGGCACAT TCAGGTGAGG 1860
CCTGAACCCT CATTACTGAG TGAGTGCTGA ATGTCAAGGA CATGTGCACA GTATTTAGAA 1920
AGTATCAGCC GGGTGTCCAC CTAATGGTGC CCTGAAGGCA GATCCTGCTA TCTGGATTCA 1980
CATAACAGGC AATGATTATA TTTCATTACT GCTTAAGTTA GCCCAGAGTT 2030