EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS108-16853 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr17:39803650-39808080 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr17:39804312-39804331GAGCGCCCTCTGCTGGCCA-8.64
HEY2MA0649.1chr17:39804652-39804662GGCACGTGTC-6.02
HSF1MA0486.2chr17:39803951-39803964GAACTTTCTAGAA-6.41
HSF1MA0486.2chr17:39806914-39806927TTCTAGAATGTTC+7.34
Npas2MA0626.1chr17:39804652-39804662GGCACGTGTC+6.02
SREBF2MA0596.1chr17:39805381-39805391ATGGGGTGAT+6.02
ZNF263MA0528.1chr17:39803843-39803864GAGGCAGGGTGAGGAAGGAGA+6.04
ZfxMA0146.2chr17:39804514-39804528CAGGCCCCGGCTGG-6.11
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_03031chr17:39804348-39804984Bladder
SE_03031chr17:39806279-39810532Bladder
SE_23072chr17:39804178-39805461Colon_Crypt_1
SE_23072chr17:39805543-39816268Colon_Crypt_1
SE_23729chr17:39804285-39805404Colon_Crypt_2
SE_23729chr17:39805654-39815658Colon_Crypt_2
SE_24709chr17:39804129-39805405Colon_Crypt_3
SE_24709chr17:39805528-39806106Colon_Crypt_3
SE_24709chr17:39806691-39815714Colon_Crypt_3
SE_26280chr17:39806931-39813376Duodenum_Smooth_Muscle
SE_26572chr17:39804188-39805339Esophagus
SE_26572chr17:39805512-39817935Esophagus
SE_28152chr17:39804166-39805384Fetal_Intestine
SE_28152chr17:39806798-39813777Fetal_Intestine
SE_30443chr17:39806910-39808843Fetal_Muscle
SE_31558chr17:39804294-39805454Gastric
SE_31558chr17:39806717-39815780Gastric
SE_33881chr17:39804203-39805423HCC1954
SE_33881chr17:39805649-39813664HCC1954
SE_35148chr17:39803583-39814501HeLa
SE_35867chr17:39803719-39814849HMEC
SE_42646chr17:39805765-39815519Lung
SE_50351chr17:39803561-39805415Sigmoid_Colon
SE_50351chr17:39805502-39813786Sigmoid_Colon
SE_52437chr17:39804214-39805417Small_Intestine
SE_52437chr17:39806280-39813892Small_Intestine
SE_55466chr17:39806823-39808013Thymus
SE_57399chr17:39804201-39805123VACO_503
SE_57399chr17:39806909-39813679VACO_503
SE_57969chr17:39804383-39805089VACO_9m
SE_57969chr17:39807424-39808043VACO_9m
SE_64297chr17:39803480-39816383NHEK
SE_65870chr17:39803512-39806328Pancreatic_islets
SE_65870chr17:39806563-39808556Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr173980370939803800
chr173980650339806899
chr173980438039805400
Number: 2             
IDChromosomeStartEnd
GH17I041647chr173980365839805837
GH17I041649chr173980600839815787
Enhancer Sequence
GATTTTCTCC TCCCTAGTCG CCTCCCCCAG TAGTTGATGG CGGCTGCCAC ACCTCAAGCC 60
AAGCAGGGGA CCTGGCAGTG TTCACCCGCC AGCTGCGTGA ACGCCCGTAA CTCTTTACGG 120
CAGAAGACCA AGGGTGCGTC TGGTCCTCAG AACTGCAGGA TGCACCGGCA GCGATGGAGA 180
AGCCTCCTTG GATGAGGCAG GGTGAGGAAG GAGACCAGAC AAGCAAGTCC TCCTCCCAGA 240
GGCAGGGACA GGAAGCAGGA GCAAGGGGCC ACCAGGGAAG CTGCAGGGGC TAGAACCCAG 300
GGAACTTTCT AGAAAGGCTA GCTGGCCCTA ACAGACCCCT GGCCTGGAGG AAGACCTCCA 360
GGGCAGGTTA GGCGGGCCAG TCACATCTCC GGGGGTGATT TAAAAGGCAC CACCTTGGGA 420
CAAAAGGATG GAAGCATTGA CCAGACAAAT GCCTGACCCG GCAGCAGCAG AAAAGGATGC 480
ATGGAACCCT GTGGGGTTCC CACCTCATGA GGTCGTCTCT CCTCATTCTT GTGCTCGGTG 540
GCTCCCAAGG GGCAGGCTCT AGTGCTCCCC ATGGAGACCC CAGGCCCAGC CGCCTTCCAA 600
GGCTCATGCC CTGTTAAACG GGGACACGCT CCGGCCGCCC GGGATCCCCA AATCTGTAGC 660
AGGAGCGCCC TCTGCTGGCC ATCTTGGGTG GCGCCTCTGC GCTGCAGTCC CGAGAGGAGC 720
CCGCGAGGCC GCGGGAGGAA TGCAGGGACC CTGGAGACCC ATCCTCCACC TGCGCTCTGC 780
AAACTACTCC TTCTCCCCCA GGGTCCTGGC TCCTCCTCGC CATCTTCAGC TTCACCGTCT 840
CTAGTCCCTT AACAGCCAGA GCACCAGGCC CCGGCTGGGC CGTGTGTCCA TGCCTCTGCC 900
TCCAGGCGCA TGGACACAAC ATTCCCTTCT GAAGCTGGCC TGCGCTGTGT ATCACCCCCT 960
ATCCCCCATC CCTCCATCTC AAAAAAGCCC TTCCCTGCCT TTGGCACGTG TCCCTCCCCC 1020
ACGCCCACCC GCTCAAGTCC CTCTGTTAAT AAACTGCTAA CCCCAAAACC AGCCTTCCCT 1080
CCAGCTTGCC CGGCCCCGAG TCTGAGGGTC CCTGGAGCAG ACACGCTCCA CCCGCGGGGA 1140
CCTCTCCCTC CTGTCAACTC CTGAGGAGCG GCAGCGGCTT CTGGGCTTCC CACGCGGGGT 1200
GTGACACCAA CGGGGGACAT AATACAAACG AACGAGGGTA AAGTCCGTGT GCACACCTGT 1260
GCATGGCCAC ATGCGGATGT GCGTCCAGGC GTGCCTTGCA GGTGTGTGGG CAGTGACTGC 1320
GCCCACCCCT CTGTCGGGTC TCGCCACGCT TAGCTGGGTG GGCTCCTTCC AACCCAGGCT 1380
GGGGCTGAGC AGGAGGAAGC CGCGGCCTCG CCCCCAGAGG GCAGCACTGA GCTGTTCTGG 1440
CCCGACTGCT GCCAGACTCT ACCCGGAGAG GAGTCCTGAG TTTCCCCGTC CAGGGCCTGG 1500
GGGAAGGACT TCAAATCTGT AAAGGAAAGC AAGGAATCAA ATCCCAAATC CAGGCTAGCG 1560
GTTACACTGC GGGCAGAGCG CGAGGCGCAC ATCGAAGCTA AAATGTCCAA AATTGGGCAG 1620
TGGATTCACG GATGTTTGTT GTGCTTTTAT TCTTTTTTTG TTTTTTTCTT TTTTTTTTTT 1680
TTTTTTTTTT TTGAGGTCGA GTTTCACTCT TGTCGCCCAG GCTGGAGTGA AATGGGGTGA 1740
TCTCGGCTCA CTGCAACCTC CACCTCCTGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCC 1800
AAGTAGCTGG GATTACAGGC GCCTGCCACC ACGCCCGGCT AATTTTTGTA TTTTTAGTAG 1860
AGACAGGGTT TCACCATGTT GGCCAGGCTG GTCTCGAACT CCTGACCTCA GGTGATCCGC 1920
CCACCTCGGC CTCCCAAAGT GCTGGGATTA CTGGCGTGAG CCACAGCGCC CGGCAGTGCC 1980
TTCATTCTTA AATCCTACAC ATATTTTGTA AATATTATTT TGAATCTATT CAGTATTACT 2040
CTTTTCAAAA TAAAGGCCTC CGAGCCCTCT CTAGAATGTG GAAAGACCAC TCATCGCTCA 2100
GTGGAGCAAA GTGAGCCTAC AAGCTCCCCA GATCGCCCCC AGAACCCCCA GAATGCAGAG 2160
GGCTCTGAGT GTCTCTGGGG TTGCCTGTGG CTTTGGGGAA GGGGAGAGCC TGGACCCAGG 2220
CTTCTTTACC GCCCGGAGTC CCGGGTCAGC ACTCCTGCAG GATAAGCCAC ACATCGACAC 2280
GCAGCTCACA CACACACACA CACACTTCCA GATTCATACA CAGGTGCATG CTCACAGGTT 2340
GACACACACA TGCTCAAAGA CTCATACACA CACGTTCACA CATAGCTCAC ATGCACATAC 2400
ACACACACAT TGAGACTCTC AGACACACAC AGACTGATAC ACGTACATTC ACACACAGCT 2460
CATACGAACA TTTACACTCT CAAATTCACA CACAGGCACA TGCTCACAGG CTGACACACA 2520
CTCAAAGACT CATATACACA CATTCACACA CAGTTCACAT GCACACTCAC ACTCCCAGAT 2580
TCACACACAG GCGCATGCTC ACAGATCGAT ACACACACAC TCAAAGACTC CTATATACAC 2640
ATTCACACAT AGCTCACAGG CACATCCACA CACACACATT GACACTCTCA GACATGCGCA 2700
CACACAAAGA CTCACACACA CACGTTCACA CACAGCTCAC ACACACACTC CCAGATTCAC 2760
ACACAGGCGC ATGCTCACAG ATACACACTC AAAGACTCAT ATACACACAT TCACACACAC 2820
ATTGACACTC TCAGACACAT GCACACACAA AGACTCACAC ACACGTTCAC ACACAGCTCA 2880
TACACACACT CACACTCCCA GATTCACACA CAGGCACATG CTCACAGGCT GACACACACT 2940
CAAAGACTCA TACCCATTCA CGTGCCGCTC ACATGTACAT TCACACACAT ACACTGACAT 3000
TCCCAGACTC ACACACACCA GCACATGCTC ACAAACTTCC CCATACTCAC AAACTTCCCC 3060
ATACTCACAC TCACACTCAT AGACTCATGT CCACACTGTC ACCCACTCAT GGACACACGC 3120
GCAAACTTTC ACATTCACAC AACCTCTCAC GGGTACACAC CTTACACACT CACACAAAGA 3180
CGCCATTGCC ACTCTGGCCT GTTAATCTTA CATCCTCATC AGGAAAGAGG AGGGGCTTGT 3240
ATCCTCCCTG ATTGCAAGAG AGATTTCTAG AATGTTCCCA GGAGACCCCA GTCCCAAGGT 3300
AGAGGGATAT TCCTCCTGGA CTGGAGGAAG CAGAATCGGG GCCAGGACTG GGCCTCAGAG 3360
GAACTCCCCG GGCTTCCTGT ACCCACTCAC TAGCTCATCC TCTCACTCCC CAGCCCATAC 3420
GTGGGAGAGC CTGACCTGGG GACATGACAG GGGACACACA GCAGGCCCTG ATCTTGGGGA 3480
GCTCCTGGAC CTCACGAGAC ACCGTGGAGA CCTGTGCAGG CTGGCCTGTG GGAGTGCCCA 3540
TGAGGGGTCC CTGACCCAGC CTCAAGGCAG GACAGGTGGG GAAAGGATCT GAGCAGGTCC 3600
AGCACAGCAG GAGACACAGG AGATGCCGGC CTTCCAGGCA GGGTGATGGG CACATGCCAT 3660
GGCAGGGGGC ACCCTCAGGG AAGCATGAGA TGTCCCAGGC CAGGGGAGCT GGCTGGAAAG 3720
GCAGGGGGTG GGGGCTGGGC CTGGCAAGGT GAGCAGGGGC CCACCTGGGA GAGGCCCACC 3780
TGGGAGAGGC CCTGCGTGCC ACACGAGGGA GCGGGGCCTT GCTCCTGAAA GCCACAGGGA 3840
GCCCTGATTA ACTGCACAGG ACAGGAGAGG ACACAGCTGC TCTGCAGAGG CACACAGCTT 3900
GTACCCAAAA CCTGCAGGAG GGCAGGTGGT CCTCAGCCTC CATTCCAGGA GCAGAGCAGG 3960
CCCAGGAGCC CACCACTGGT CCAGGGAAAC CCCCCACAGG TACAGCCACG TTCTTCCCTG 4020
ATTCATCACA ACGAGGCCCC TGTAAGTGAC AGAGGGTCGG TCTGTGCAGA CCTGGAAACA 4080
CACGGCCCCA AGACCTGGGA TCCTGAAGAA GCAGTGCCAG CTCCTCCCAG ACAGCCCGCC 4140
CCAGCTGGCC CGCTGGCTCC AGCCCAGCCA GGAGCGAGGG CAGTGGGGGA GCCCCACAGG 4200
AGGGAACGGG GGCTCAGGAG GCCTGGTGGG GCAGAGCTGG GACAGCTGGG CGAAGGGGCT 4260
GGGTCCTGGC TCCGCGACGA GGGCCCATTC CTGGGTGAGG GAGGGTGGGG CAGCCCACAC 4320
ATTCCAGCTG CTGCCGCTCC CGCCAGCCAG TACCAGCCTG TTCTCGCCTG TTCCCACTAG 4380
GTCCCAGGCT GCCCTGGGCC CAGCTCCCAG TGCCAGCTCC CAGAATCCTT 4430