EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS055-06726 
Organism
Homo sapiens 
Tissue/cell
FT33 
Coordinate
chr5:77799710-77801960 
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: 2             
ChromosomeStartEnd
chr57779979577800221
chr57780022577801516
Number: 1             
IDChromosomeStartEnd
GH05I078503chr57779962577808076
Enhancer Sequence
ATACAGCCTG GAAGCAGAAC TCAGCAAGTT GTAGACCTGC GTCTACAGGT CTCTGCACAT 60
AGTAGGCATC CAATACAAGT GCCTAGGACT GAAATTGAAT TCTGACCTAC CTTCTCATAA 120
CATGTCTGCA TTTTTTTTAC TTTTTACCAA GGGACTACTA AAGGCTGATG AATTAGGAAA 180
TGTGTCCTAT CAGTGGTATT TTAAAACTGA TTCAGACACG GAACTGTTGG ACCTGACTTC 240
TGGTGGAGCA TCATCTGTCT GGACAGCCAG AAACCAAGAG CCTCCCTTTG GCAGCCAGAA 300
GTCCTCAGGG CCTTGTGCTC ACCAGGAACA AAAGGAAGGG CTGTTCCCTC TACTCTCCCC 360
ATGCCTCTTT GAGGGTGTTC TGAAGGTGGG CAACCAAGGT CACACCACCC CAGAGAAAGC 420
CCGGTGACTT TTTCAGGAGA AAAATTCTGA GGCAGGGCTC CATGTGTGCC AGGCATCTCC 480
GTCCATCTCC CTATGCTTCC CAAGCCCCTG TTCTGATTTC TCTCCTCTCA GTGGCTGACC 540
TTGTCTTTTG GGCCTGAGAG TGAATGAGTA GGGCATGAGA TCAGTCATGG GGTTGGGCTA 600
TGGTCATAAC CTTGATGCTT AAGGTGATTT TTTACCCTGT GTAAAAAGCA GTAAGAATAC 660
CAAATCCTGG AGAGTGATCA GCTGCATTTC GTATGCCCAC CCATACTTCC ATGCATCAGA 720
TTTATGACAA AAGCAATTAT ATAAGCAGCA AAGGCAAAAC CCCCACGTGT CTGTCTCTGC 780
TTTTCCTTTT ATTGCTTTTT TTCATGTTGT CCTCTTTCAC CCTCAATCAT TGCTCACTTC 840
CAAGAAGGCT GAGCCTGCAT ACACCAGGCC CTTCACCGCC ACTGCCAGCG CCATTCCCAC 900
GACCACACAC CCTTCACCCC AGCCCTGCAG AGGCAGGGTT CAGCCCCAGG GCAATCTATC 960
TGGTCAGACT GGTGGGGCAG CTTGCTAAGG CTGTCCTGCT GGACTGAGAC CCATGCAGGC 1020
AGAGGGCTGG AGGGAGTAGA GTGTGAGAGC CAGCCCAGCA TAAAGGGAAG ACTGGAAGAT 1080
AGCAGGCAGC TGGCCGGTGG CTCATGCTTA TGGCAGTCCC TGTGGAATAG GCCCAGCCAG 1140
CACAAGTGAG CCAAATCCTG AGCTCAGTTT AATGGCTTCG GTCCCAAACC TGAGTCACTG 1200
GGGATTCCAT GGACTTCTAA GAGAGCCCTA CACGCATTTC CAAAAACAAA CTGCTTGATG 1260
TTGTCATGGA AAACCTGGAT CTTTGCATTC TATGGTTTCA CGATGGATTA CATCCAGGTC 1320
ACAACCTAAG GAAGACAGCT GGCAAAAAGC CAACCCTGCT GGCTGATCAC CCGGCTTTTG 1380
TAATGAATCC CAGAGGGATG CAAACTGATG TGTGTTGCTG CCTCTGCCAA GTCCTTGGAC 1440
AAGTTCTCAC CTCATGAAGA CTAATCAACC TGTGATTTAC TCCGCCAGGA GAATCTCAGA 1500
AGCCACCTGC AATCAACACT CAACGGCTAG AAGCTGCCTC CAGAAAGAGA AGGAATGGAA 1560
AATGTGTGTG TCAGGGGAAG GGGAGGGGGA GGAAGGAGCT CTGTTTTCTT GTCAATTTGA 1620
CTGCTCTCTC CTGCCTTTTA AAAAAATGAT CTGAGGACAC CCCTGGTTAC ACCAAAGCCA 1680
CAGGACTGCT GTGCACCCTG AGCTCCAACA CAGGCAGGCT CTTAAGGACA GGGAAGGCCC 1740
CTACACACTG TATTTGTGTT TGATTGGAAC AGAGTAAGGT CAATTCTAAA AGCTACAAGA 1800
TATCCCTGTT CCGTAGAATG CAACAAATCC GGGAAACAAA TAATATACTA AAACTTGCCA 1860
AGAAAGCAGA AATACTTTGA TAATGATTCT ATAGCTACCA TTTATTATTT ACTGTGTGTT 1920
AAGCACTATG CTTAAGCCTT TCTCATATAT TATCTAACTT AATCCTCAGA ACAGTCCTGA 1980
GGTATAAACC TATTGTTATG CCCATTTTAC AAGTGAGAAA ACTATGGTTC AGAAAAGTGA 2040
GGCAAATTGG TCCGTGTTTC ACAGGCACAT TCAGGTGAGG CCTGAACCCT CATTACTGAG 2100
TGAGTGCTGA ATGTCAAGGA CATGTGCACA GTATTTAGAA AGTATCAGCC GGGTGTCCAC 2160
CTAATGGTGC CCTGAAGGCA GATCCTGCTA TCTGGATTCA CATAACAGGC AATGATTATA 2220
TTTCATTACT GCTTAAGTTA GCCCAGAGTT 2250