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

TagContent
EnhancerAtlas ID
HS051-13455 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:4086230-4090310 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs239996chr194089980hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr19:4087891-4087906TGAACTCCTGACCTC-6.22
SP3MA0746.2chr19:4086815-4086828GGTGGGCGTGGTG-6.48
SP8MA0747.1chr19:4086815-4086827GGTGGGCGTGGT-6.32
ZfxMA0146.2chr19:4086856-4086870GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_02962chr19:4088245-4088724Bladder
SE_02962chr19:4089108-4090268Bladder
SE_04051chr19:4088988-4089778Brain_Anterior_Caudate
SE_06913chr19:4089013-4090455Brain_Hippocampus_Middle_150
SE_09464chr19:4088623-4090988CD14
SE_12453chr19:4087961-4088833CD3
SE_12453chr19:4088930-4090538CD3
SE_19502chr19:4088861-4090347CD4p_CD25-_Il17p_PMAstim_Th17
SE_20194chr19:4087780-4090691CD56
SE_22707chr19:4087486-4090724CD8_primiary
SE_23073chr19:4086192-4087252Colon_Crypt_1
SE_23728chr19:4086220-4086917Colon_Crypt_2
SE_23728chr19:4087953-4088512Colon_Crypt_2
SE_24683chr19:4086187-4086913Colon_Crypt_3
SE_24683chr19:4087849-4088694Colon_Crypt_3
SE_24683chr19:4089265-4091298Colon_Crypt_3
SE_26575chr19:4086174-4086969Esophagus
SE_26575chr19:4088886-4090351Esophagus
SE_27700chr19:4086249-4086769Fetal_Intestine
SE_28696chr19:4086235-4086995Fetal_Intestine_Large
SE_31428chr19:4086175-4087238Gastric
SE_31428chr19:4089072-4090640Gastric
SE_42412chr19:4088946-4090861Lung
SE_48938chr19:4089030-4090276Right_Atrium
SE_50061chr19:4086157-4087380Sigmoid_Colon
SE_50061chr19:4087804-4088704Sigmoid_Colon
SE_50061chr19:4088942-4090700Sigmoid_Colon
SE_53358chr19:4088933-4090471Spleen
SE_55380chr19:4089055-4090659Thymus
SE_62529chr19:4051126-4090382Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1940881914088358
chr1940895064089868
Number: 1             
IDChromosomeStartEnd
GH19I004086chr1940862414091270
Enhancer Sequence
TTGGCCTCCC AATGTGCTGG GATTATAGGC GTGGGCCACT GTGCCCAGCC CTTTCTATTT 60
AAAATGTTTT AACAGGGAAA TCCTGCTAAA ACTGGGAAAT GTACATTTCG TCTGGGGTGC 120
AATGTGCACA TTGGGTTGGG GTGGCAGGGA TGGGGACAGG ACGGGGACGC TATGGCGTGG 180
TGCCCCGCGT GGAATCTCAC CCTCTGGGCG GCTGGTTGCT TCTCCGGCCT CATTTCATTT 240
GATGACCTTT CCACTTGCCC CACCCCGAGG CGGTTGTTGC AGGAGGAGAA GGAAGTATGT 300
GCCTGTCCCA GGGCCGGCCT GGGTCCCACC TGGGGAGAAT TCCACAGGAT GAAGCGAGCA 360
GGCAGTCGCC TGTGACCCCA GCTTCATAAA TCAAATATGT TAGCAAATCC TGCCCGGCAC 420
ACAGCCTGGG GCACTTGCAT GGAGCCAGTG ACTTTTTGGT GTGTCCGGGG ACAGACTGCA 480
CTATGGAGAG GGATGTCAGG GCTGCCCATG CTCTCCGGAG GCAGAAGCCA GCACATATGA 540
GCAAGTCAAG CGCTGTTTAT TTACGATGAA AATACCAAGC TGGGGGGTGG GCGTGGTGGC 600
TCACGCCTGT AACCTCAGCA CTTTGGGAGG CCGAGGCGGG TGGACGGCTT GAGGTCAGGA 660
GTTTGAGACC AGCCTGGGCA ACATGGTGAA ACCCTGTCTC TACTAAAACA CAAAAATTAG 720
CTGGGTGTGG TGGGCACCTG TAGTCCCAGC TACTCGGGAG GCTGACACAC AAGAATCAGT 780
TGAACCGGGA GGTGAAGGTT GCAGTGAGCT GAGATTATGC CACTGCACTC CAGGCTGGGC 840
GACAGAGCAA TACTCTGTCT GGAAAAAAAA ATACCGAGCT GGGAAAACAG CCGACAAAAC 900
ACTGTAGGAG TCTTCTTGGG GCCACAGGTG GTGTGCCCCA GGTCCACGTG GGCCTCAGAC 960
ATGGGGGCAG GGCTATCATG TTGTCGAGAA GTTTTTTTTT TTTTTTTTGA GACAGAGTCT 1020
TGCTCTGTCG CCCAGGCTGG AGTGCAGTGG CGCGATCTCG GCTCACTGCA ACCTCCGCCT 1080
CCCGGGTTCA AGCGATTCTC CTGCCTCAGC ATCCTGAGTA GCTGGGACCA CAGGCGTGCT 1140
ACCATGCCTG GCTAATTTTT GTATTTTTAG TAGAGACAGG GTTTCACCAT GTTGGCCAGG 1200
CTGGTCTCGA ACTTCTGACC TCGTGATCCG CCCCTCTTGG CCTCCCAAAG TGCTGGGATT 1260
ACAGGCATAA GCCACCGCTT CCGGCCTATC TGGAGGTTTT TAATAACCAC AGAAAACCTC 1320
AACACGTCTG TGTAAAACCT TCCAATGTCA AGGAGTGAGC TGCCCCAGGG CCCCCCAAGG 1380
CCTGGCTTTC AGTGACACTC CCTTCACCCT AAAGCCCCGC AAACGTTATT TATTATTTAT 1440
TTTTTATTAT TTTTTTGAGA CGGAGTCTCG CTGTCTCGCC CAGCCTGGAG TGCACTGACA 1500
CAGTCTCAGC TCACTGTAAG CTCCGCCTCC CAGGTTCACG CCATTCTCCT GCCTCACCCT 1560
CCCCAGTAGC TGGGACTACT GGCATCCACC ACCAAGCTCG ACTAACTTTT TTTTGTATTT 1620
TTAGTAGAGA CAGGGTTTCG CCGTGTTGGC CGGGCTGGTC TTGAACTCCT GACCTCAGGT 1680
GATCTGCCCA CCTTGGTCTC AAAGTCCTGG GATTATAGGC GTGAGCCACC CAGCCCATGC 1740
CCTGCAAATT TTAAAATGCT GCATGTTTTA CAGGAAAGGG TCTGGCCCCG GGAGGCAGGG 1800
AAATCCTACC CCCTGGACTG CAGCATGTCC GTGGCCAGGG CAAAAAGGGG CATCCCCAGG 1860
TGTGTAGCCA CCTTTGGGAG CACCCGGGAT CCCTTCCCAG GCCTCCACAG TGGAGAAAAT 1920
GAGGCAACGA GTCCAAAGGA CAGCAGGCAG GAGGGGGATC TCGGATGAGG CGGCGGCTGG 1980
GTCTGGGAGG TTTCTTGGGG GAGCAGGAGT TGAGAGATCT AGAAACCGCC AGGGTGGACG 2040
CACTCTTGCC ACATCTACAA AGTAGTTTCT AGAAGTCTGA CCCTGAAGCG AGGCAGGGAA 2100
GATAGGCAAG ACCACGGCTT CTCTCCCGTC CTTCCCTCTG GGGTGCCGTG GGGCTCCAAT 2160
GAAGCTGCAG GATGGCTGCG CACACCGCAG GGATCCTGGC GCGGGGTCCA TCCCCACCTA 2220
GCCCAGACTG CCCCTGCTCC CCTGGGACTC CGTGTCCTTT CATTCCTTGC CAATGGCAGG 2280
GGGTGGCCGG GACCCTGGGG TTTCCAGGAC CGGCCGAGGT CCCGCCGGTT TGGAGCACAG 2340
GCAGCCAACA CATTCCCCCC GGCCCTCCCG GCAATCCTGA GGGTCCTGGT TACCCACAGG 2400
GCGGCACCTT CAACACTTTT TTTTTTCTCC TATTTTTTAT TTTTTGGGGC CACACTCCGT 2460
CGCCCAGGCT GGAGTGTGAT GGTGAGATCT TGGCTCACTG CAACCTCCAC CTCCCCAGGC 2520
TCAGGTGATT CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA CTACAGTTGT GCACTACCAT 2580
GCCCGGCCAA TTTTTTTTTT TTTTTTTTTT TTTTTTTGTA GAGATAGGGT TTTACTATGT 2640
TGCTCGGGCT GGTCTTGAAC TCCTGGGCTC AAGTGATCTT CTTGCCTCGG ACTCCCGAAG 2700
TGTTTAGATT ACAGGTGTAA GCCACCAAGC CTGGCTTTTT TTTTTTTTTT TTTAAGTCAT 2760
GTGAGACTTT AGGGCAAAAC ATAAAGGAGA GCAGCCTGGG GAGCTGTTTG CAGGAGGTGT 2820
CAACTCATCT CTTCTTTGGT GTCTGCAGAA AAAAAAAAAA AAAAAAAGCC ACACAAGACT 2880
AGAAGGGTCA CCCTAAGAAG AAAAGGACAA TCCAGCAGTT CCCACAGAAC CACAAGCCCC 2940
CACCTTCTGC TTTGTTTCCT CCAGAAACAC AGTTGCCAGC CACCCTTCCC CTACAATTCG 3000
CCCGCAGATA ATATCAGCTT GCTGGTAGTC TCCAGGAAGT ACTGAAGGGG GAGGCTCACA 3060
GCCTCAAGAG CTTTAGAGAG CTCAGAGGGA CCCTAGAACA GCCCAGCTGC CCACCACACC 3120
TAGCCCAGAG GTGGCCTCCT CTATCCGAGC ACACAGTCCC GAAGGTAGAA AGGCTGGGCT 3180
TTGGATCTCG GACAACCGGA GAAGCAGGCG ATGGGCCTCC GGGAACCCCG AAGACCCCAG 3240
GACAAGCCCT CACCGTTTCA TCTGCAGCCC ACTGCGGCGG AACAGTTCAA AGGCCCGAAA 3300
GTGTCACATG CCCTGGTGGT CACTTCTGAT TTGTTGGGCG AGGAGAGGTG ACAGAACCAC 3360
CCGCCCTGGG CTGGGCCTGC TGCGGACGCA GGGGGAGTGC AGGGCGTGTC TCGGGACCTG 3420
CTGGGGTTTC CAACCAAACC GACAGCTTGG AAAGCCAGCG CTTCCTTTCT GTGGGGCTGA 3480
GTCTCAGCTC AGCTGCCACT GCTGGGAGCC CCCACTCCCT GAAGCGGGGG GACAGGGAGA 3540
GGATGGTGCC ACGCTGGGGA AGAGGCAGGG GCGGCCTTCC CGCGGAGGCT ACGTGACAGG 3600
AGCAGTGTAG AGGAAGTGGT TTCCATCACG GAAGGCCGAA GCTCTGCCTT CCACAGGGGC 3660
AGAGATGGTG GCGGGGAGGA CACAGAGGGA AACCAGGTGG CATTTCCCTT CTTTTTTTTC 3720
AGTAGCCTTG CTCTGTCACC CATGCCGGAG CGCACTGGCA CCATCGAGGT TCACTGCAGC 3780
CTCAATCCCC TGGGTTCAAG CGATCCTCCC GCCTTAGGCT CCCAAAGCAC TGGAATGACA 3840
GGCATGAGCC GCCGCCCCCA GCCTCACTCT CCTTCCTTTT GGTGAGAGCC GCCATCGCCT 3900
GGGGGCTCAC TGCAGGTCTT CATCCCTTGA CCCAAAGGGA GAGGCGAGCT CTCCCTAAGG 3960
GAGGGCCCTG CGCCCTCCAG CCTCGGCGCC CGGCGATGCG GGTCAGCTCA GGGATGTCCT 4020
CTCCGTGCTG GGCTGAAGCA AAGCCCAGCA CCCAACGCCG AACGGAAGAA AGAAGCAGGA 4080