EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS175-11880 
Organism
Homo sapiens 
Tissue/cell
SK-N-MC 
Coordinate
chr17:75317610-75321850 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs73997493chr1775319800hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F1MA0024.3chr17:75321268-75321280TTTGGCGCCATA+6.52
E2F1MA0024.3chr17:75321268-75321280TTTGGCGCCATA-6.62
E2F3MA0469.3chr17:75321266-75321282CTTTTGGCGCCATATC+6.69
E2F3MA0469.3chr17:75321266-75321282CTTTTGGCGCCATATC-6.7
E2F4MA0470.2chr17:75321267-75321281TTTTGGCGCCATAT+7.82
EBF1MA0154.3chr17:75318659-75318673AGTCCCTGGGGAAG-6
GFI1MA0038.2chr17:75320058-75320070GAAATCACGGCA+6.32
HNF4GMA0484.1chr17:75320489-75320504TGGCCTTTGGCCTTT-7.21
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_01003chr17:75314471-75320881Adrenal_Gland
SE_01003chr17:75321234-75322263Adrenal_Gland
SE_02573chr17:75314852-75322355Astrocytes
SE_23085chr17:75318582-75320199Colon_Crypt_1
SE_23085chr17:75321226-75322766Colon_Crypt_1
SE_23764chr17:75318647-75319239Colon_Crypt_2
SE_23764chr17:75319472-75320169Colon_Crypt_2
SE_23764chr17:75321349-75322628Colon_Crypt_2
SE_26523chr17:75317620-75320998Esophagus
SE_26523chr17:75321011-75323016Esophagus
SE_27912chr17:75317827-75320716Fetal_Intestine
SE_27912chr17:75321111-75321907Fetal_Intestine
SE_28804chr17:75318168-75320679Fetal_Intestine_Large
SE_28804chr17:75321128-75322107Fetal_Intestine_Large
SE_31375chr17:75317719-75320861Gastric
SE_31375chr17:75321013-75322560Gastric
SE_34459chr17:75314126-75322198HCT-116
SE_44207chr17:75314415-75323298NHDF-Ad
SE_44898chr17:75314704-75322666NHLF
SE_45842chr17:75314273-75323403Osteoblasts
SE_47165chr17:75306266-75330553Panc1
SE_50053chr17:75317752-75320976Sigmoid_Colon
SE_50053chr17:75321006-75324453Sigmoid_Colon
SE_52347chr17:75317968-75320779Small_Intestine
SE_52347chr17:75321139-75322451Small_Intestine
SE_53286chr17:75314497-75322399Spleen
SE_55839chr17:75317662-75322544u87
SE_60329chr17:75311573-75340182Ly4
SE_65185chr17:75314330-75320112NHEK
SE_65353chr17:75314145-75324695Pancreatic_islets
SE_67611chr17:75317662-75322544u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr177531967075320031
chr177531820675318391
chr177531859575318736
chr177531902875319523
Enhancer Sequence
AGCTGGGACT ATAGGCGCCC GCCATATTTT TTTGTATTTT TAGTAGAGAT GGGGTTTCAC 60
CGTGTCAACC AGGATGGTCT CGATCTCCTG ATCTCGTGAT CCGCCCGCCT CAGCCTCCCA 120
AAGTGCTGGG ATTACAGGCG TGAGCCACGG CGCCCGGCCT CAGGGCCACA TCTTGATTGT 180
CACGTTGGGA CTGGTGGAGC GGGTGTGTGT TGTGCCGCTG AGCACACCCA GTCGGGCACA 240
GCAGGCGGAC CTCAGGAGGG GGCCAGGGGA GACGGCAGAA GGCTTGGGTG GCAGTGAAAC 300
TGCATCTTAT CTGTTTGAGC TCGGGGGCTC AGGCCCGCTG GGACGGGTGG GTGTGGAGCC 360
CAGCGTCCTG CTCTCCGCCC AGCAGGAGCC GCAGGGCAGG GAGCGCTGAG AGGGACCTTC 420
GTCAGGCTTG CACAGTGGAG CCGTCCTCGG AGTGACCACC CCACCAGGCA GCCTGGGCAG 480
ACCACAGTGG GTCCCCTGCC TCCTGGGCCA CCAGCCCCAG GAGGACGTCA CTCCACCCGC 540
CTGGCTGGCA GGGGCCTCGG GGAGCCTCGG GTTCGGCCTT CACTTTATAG ATGATCTAGC 600
CGAGGCCCAG ATGGGTGACC AGCAGGGGAT CTGAGAGCTG AGCAGAGAGG CGTGGGTTTG 660
GGGGTGGTGC TCCCTGGGGA GCTGGAAGTG ATGGCACCCT CCCAGGCTCA CAAAACACGG 720
GCTTTTCATG AACTGAACAA AACACTCTTT GAAAGCAGCC AGTGCTGTGC CCCAGAGACC 780
ACTCTGATCC CTGCTGCCCT TGGCTGAGGA CAGCACAGCC AGGGATGAAG CGGGGACCTC 840
CCCTCGGGCT GTGCCTTGAT GAAAGATGCT TTCTACAAAA TCCCATTCGG ATGTGTTTTC 900
ATGTAAGAAA ACGTACATTT TTAGAAACTC AGTTGTAAAC TGGCTGCCTT CCGAATGAAC 960
ACGACAGTCC CGGAGCTGTT TCCCTTAATG AGGTTCTCGT CCTGGGCAAA CTTTAGCGCT 1020
GGTCTTTAAT TGTCACTGAA CTCCCGCACA GTCCCTGGGG AAGTGACTTC CTTCCTGTCC 1080
CTGCTGGGTG GCCTTGAGCA AGCCACTTGG CAGCTCTGGG CCGCAGTTCC GTCATCTGCA 1140
AGGTGAGGGG TGGGAGCGGC ACGGCCCCTA GGCAGCGCCC CCACCTCCTG CGGGTTTCTG 1200
CGCGTGTCCT GAGTTTTGTG GGCGCCTCTT CCCTCACTGA GGGGCTCTTC TTCTCTGCAG 1260
GGCATGGCTC ACGCCGCGTT GTCAGGCTGC AAGCCACTGC GAGAGCTGCT CTGATCCCCA 1320
AGCATGCTCT GGCCTGAGGA GGAGCCATGG GGAGGACGCT GTGCCTGTGT GACAGAGGCC 1380
TGCCCGGCAG ATGCCGGCCC GCTGACTTCC AGACGTGGCT GTGGGTGCCT CATGCCCCAC 1440
TGGGCTGGCG TGTGAGGCGT GTCCAGCTCA GGCTGCCCTA CAGCTGCCCA GGAAGGGTTT 1500
GTGGGAGGGG GTGGTCCTAC CCTGGTGAGT CCACGGTGGT CTGCCAGCCC CAGGGAAGGC 1560
TTAGGAGCCC CAAGACCTGC CCTCTTGTCC CTCCCTCGGC AGTGTCTGGC TCCGGTCTGG 1620
TTTGTGAACG GGGGCCTGGG TACTCTCCCG CCCTCCCTGG GGGCTGTGGC CTTCCCCTGG 1680
GAAGGTGCTG GAGGGTTTGT CAGCAGGGCC GGCATGAGTC ATGGAGTGGT GACTGGCCGC 1740
TGAGGCATGG AAGGCCACTC CTTCCAGCCA AGGGTCGGAG CTTTTTTTTT GTTCTGGAAC 1800
GGCTTTGTGG CTTTTACAAA TTAAGCAGTT TTATCTTGTT CCAAGAGCTT GTATTTCAGC 1860
AGGGAGAGAG TCTCCAAGAA GGGAACTTTC CACTGGGGAG CTCTGTTGGG CTGGGAGGCT 1920
AGGAACAGGC CACGAGGGAG GGCTGCAGGC AGGGGAAGTG GCCGTCTGTG CATGGTCATG 1980
AATGCAGGCC CGGGGTCCTG GAGGGGGCTT GGCCACGCTG TCGCTGGACG TCTGTCCCCA 2040
CCAGGGTCCA TCTGATGCAG TACGGCACAG GGTAAAGCCC AGCTCCTCTT ACGGGGTTCC 2100
TGGGTCATCA GTGGGCGGGG AACCGAGGCC TCCTGGAGGG CGGTGCCTCA GCCCTCACCC 2160
CTCCCTCCTG TCCCTCGCTG TGCTGTCCCC GATGGCCTCT GCCATCCCCT GGGAGTTCTT 2220
ACCCCTGGAC GCTCGGTGCC TGTCCGGTCT CAACCTCTCC AGCTCTGCTT TTCCATCTCC 2280
GAGGTGAGAG GCCTGGCCTG ACGCGCTCTG CACCCGCTTC CTGCCCAGCC CCGTGGGAAC 2340
TCTGGTCCCT GTAGTGGTTT CCTGGGGCTG CCATCACCAA GTGCCACAAA CTGGGTGGCT 2400
CAAAACACCA GACATTTCTT CTCTCGCCGT TCTGGAGGCC AGAAGTCCGA AATCACGGCA 2460
TCAGCAGGCC TGGTTCTTTC CGGAGGCTCC GAGGGGGAGC CTGCTTCTCG CCTCTGGCAG 2520
CTTCTGGCGG CTCCCGAAAC CCTTGGCGTT CCTTGGCTCG TGGCCACACC ACTCGACCTC 2580
TGCCTCCGTT GTCACGGGGC CTCCTTCTGT GCCCTAAATC TCCCCCTGTC TGTCTCTCAT 2640
ACGGACAGTC TTTCTCGGAT TTAGGGCCCA CTGGGTAACC CAAAATGGTC CCATCTCAAG 2700
ATCCTTAACT TCATAACGTC TGCAAAGACC CTTTTTCCAA ATAGGCCATG TTCATAGGCT 2760
CTGGGGTGGA TGTAAATTTT AGGGGCCACC TTTCATCCCC CTGTTGTCCC CGTGTGTCTG 2820
GATGCACAGC ATGGTTCCAT GTCCCAGACT CCTTGCTGGA CCCCTCTGGC CCTTTGGGGT 2880
GGCCTTTGGC CTTTTCCACT CGTTTCTGTG CTCCTGGTGA GGTGTCGGGG TCGGGCTTAG 2940
CCCCTGCAGG AATTCTGGGG ACAGCATGGA GCCGGCAACT CCCCACCAGG CGTCTTCCTA 3000
CCTGCCCAGA GCTCATGGTT GTGAGGGGTC TCTCCTTGTG GTTTTGATTT GCAATTCCCC 3060
AGTGGTTAGT GATGTTGAGC ATCTTTTCGT GTTTATTGCT CATTTGCACA TATTCTTGCA 3120
GAAATGTCTG TCCAAGTCCT TTACCTGTGT TTGATTTGGA TGATTGTTGT TGCTGAGTGT 3180
TAGGAGATCT GTAGATTAAT ATCCAGATAC TAATCCCATA TCTGACCTAT GATTTGCTGC 3240
CATTCCATGG ATTGCCTTCT CCCCACGTTG TTAGTGCCCT TTGATATGCA ATTTTTTTTT 3300
TTTTTTTTGA GATGGAGTCT GACTCTGTTG CCCAGGCTGG AGTGCAGTGG CATGATCTTG 3360
GCTCACTGCA ACCTCCGCCT CCCTGGTTCC AGCGATTTTC CTGCCTCAGC CTCCTGAGTA 3420
GTTGGGATTA CAGGCACCCG CCACCACACC CAGCTAATTT TTGTATTTTT AGTAGAGACG 3480
GGGTTTCACT GTGTTGACTA AGTTGGTCTC GAACTCCTGA CCTCAAGTAA TCCACCCGTC 3540
TCGGCCTCCC AAAGTGCCGG AGTTACAGGC GTGAGTCACC GCACCCAGGC TGATATGCAA 3600
ATATTTTAAA CTTCTATGAC GTTCCACTTT ATCTATTTGT TCTTCTGTTG CCTGTGCTTT 3660
TGGCGCCATA TCCAAGAAAT CATTGCCAAA TGCAACGTCA GGAAGCTTTT CCCCTGTGTT 3720
TTCTTCTAAG AGTTTTGTGG TTTTAGCTCT TGAGTTTAGG TCTTTGATGC AAGTTGAGTT 3780
GATTTTTGCA TGTGGTGTAA GGGCTGGTCC AGCCTCATGC TCTGGGCTCT TGATTCACTT 3840
CTCTTCTTTT CTCACGCCCA GCTGGTTCCG CTGGGTGGCG GGGAGGAGTG GGGAAGTCCC 3900
GGGCTGGGCC TGCACTCGAT CATCCCCTCT CAGGCCAGCC AGGGAGTCTC AGCTCCTGCC 3960
CAGGACCTGG CTGGACGTGC TCCCTACCGG GAAAGCCTGG GCCGTCTTTC TAGGCTGATG 4020
GCAGGGCCAG CCCGGGGCGT CCTGAGGCCT GCCCTGCGGA CATGCCCCTT GTTCTAGGTG 4080
GTGTGGCTGC CCGGCCTGCG TGTGAGACCA GCTGTCTGTG CTTCAGGCCA TGGAGGCTGA 4140
GTGTTTCCAG CCTGTCCCCT TGCTCGGCTC TCCCTCTGGG GAAGCCCCTG CAGCCCATTC 4200
TCTGCCTCCG CTTCTGCCAT CTGTGCCTTT GTCTGCTTCC 4240