EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-30478 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr5:77799680-77801940 
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
TGGTACAGTT TGTGAAATGA TGACTCTCTA ATACAGCCTG GAAGCAGAAC TCAGCAAGTT 60
GTAGACCTGC GTCTACAGGT CTCTGCACAT AGTAGGCATC CAATACAAGT GCCTAGGACT 120
GAAATTGAAT TCTGACCTAC CTTCTCATAA CATGTCTGCA TTTTTTTTAC TTTTTACCAA 180
GGGACTACTA AAGGCTGATG AATTAGGAAA TGTGTCCTAT CAGTGGTATT TTAAAACTGA 240
TTCAGACACG GAACTGTTGG ACCTGACTTC TGGTGGAGCA TCATCTGTCT GGACAGCCAG 300
AAACCAAGAG CCTCCCTTTG GCAGCCAGAA GTCCTCAGGG CCTTGTGCTC ACCAGGAACA 360
AAAGGAAGGG CTGTTCCCTC TACTCTCCCC ATGCCTCTTT GAGGGTGTTC TGAAGGTGGG 420
CAACCAAGGT CACACCACCC CAGAGAAAGC CCGGTGACTT TTTCAGGAGA AAAATTCTGA 480
GGCAGGGCTC CATGTGTGCC AGGCATCTCC GTCCATCTCC CTATGCTTCC CAAGCCCCTG 540
TTCTGATTTC TCTCCTCTCA GTGGCTGACC TTGTCTTTTG GGCCTGAGAG TGAATGAGTA 600
GGGCATGAGA TCAGTCATGG GGTTGGGCTA TGGTCATAAC CTTGATGCTT AAGGTGATTT 660
TTTACCCTGT GTAAAAAGCA GTAAGAATAC CAAATCCTGG AGAGTGATCA GCTGCATTTC 720
GTATGCCCAC CCATACTTCC ATGCATCAGA TTTATGACAA AAGCAATTAT ATAAGCAGCA 780
AAGGCAAAAC CCCCACGTGT CTGTCTCTGC TTTTCCTTTT ATTGCTTTTT TTCATGTTGT 840
CCTCTTTCAC CCTCAATCAT TGCTCACTTC CAAGAAGGCT GAGCCTGCAT ACACCAGGCC 900
CTTCACCGCC ACTGCCAGCG CCATTCCCAC GACCACACAC CCTTCACCCC AGCCCTGCAG 960
AGGCAGGGTT CAGCCCCAGG GCAATCTATC TGGTCAGACT GGTGGGGCAG CTTGCTAAGG 1020
CTGTCCTGCT GGACTGAGAC CCATGCAGGC AGAGGGCTGG AGGGAGTAGA GTGTGAGAGC 1080
CAGCCCAGCA TAAAGGGAAG ACTGGAAGAT AGCAGGCAGC TGGCCGGTGG CTCATGCTTA 1140
TGGCAGTCCC TGTGGAATAG GCCCAGCCAG CACAAGTGAG CCAAATCCTG AGCTCAGTTT 1200
AATGGCTTCG GTCCCAAACC TGAGTCACTG GGGATTCCAT GGACTTCTAA GAGAGCCCTA 1260
CACGCATTTC CAAAAACAAA CTGCTTGATG TTGTCATGGA AAACCTGGAT CTTTGCATTC 1320
TATGGTTTCA CGATGGATTA CATCCAGGTC ACAACCTAAG GAAGACAGCT GGCAAAAAGC 1380
CAACCCTGCT GGCTGATCAC CCGGCTTTTG TAATGAATCC CAGAGGGATG CAAACTGATG 1440
TGTGTTGCTG CCTCTGCCAA GTCCTTGGAC AAGTTCTCAC CTCATGAAGA CTAATCAACC 1500
TGTGATTTAC TCCGCCAGGA GAATCTCAGA AGCCACCTGC AATCAACACT CAACGGCTAG 1560
AAGCTGCCTC CAGAAAGAGA AGGAATGGAA AATGTGTGTG TCAGGGGAAG GGGAGGGGGA 1620
GGAAGGAGCT CTGTTTTCTT GTCAATTTGA CTGCTCTCTC CTGCCTTTTA AAAAAATGAT 1680
CTGAGGACAC CCCTGGTTAC ACCAAAGCCA CAGGACTGCT GTGCACCCTG AGCTCCAACA 1740
CAGGCAGGCT CTTAAGGACA GGGAAGGCCC CTACACACTG TATTTGTGTT TGATTGGAAC 1800
AGAGTAAGGT CAATTCTAAA AGCTACAAGA TATCCCTGTT CCGTAGAATG CAACAAATCC 1860
GGGAAACAAA TAATATACTA AAACTTGCCA AGAAAGCAGA AATACTTTGA TAATGATTCT 1920
ATAGCTACCA TTTATTATTT ACTGTGTGTT AAGCACTATG CTTAAGCCTT TCTCATATAT 1980
TATCTAACTT AATCCTCAGA ACAGTCCTGA GGTATAAACC TATTGTTATG CCCATTTTAC 2040
AAGTGAGAAA ACTATGGTTC AGAAAAGTGA GGCAAATTGG TCCGTGTTTC ACAGGCACAT 2100
TCAGGTGAGG CCTGAACCCT CATTACTGAG TGAGTGCTGA ATGTCAAGGA CATGTGCACA 2160
GTATTTAGAA AGTATCAGCC GGGTGTCCAC CTAATGGTGC CCTGAAGGCA GATCCTGCTA 2220
TCTGGATTCA CATAACAGGC AATGATTATA TTTCATTACT 2260