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

TagContent
EnhancerAtlas ID
HS083-00233 
Organism
Homo sapiens 
Tissue/cell
HCC1954 
Coordinate
chr1:202024940-202028220 
Target genes
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZfxMA0146.2chr1:202026754-202026768GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_23058chr1:202025021-202026806Colon_Crypt_1
SE_23058chr1:202026927-202028182Colon_Crypt_1
SE_23723chr1:202025104-202025610Colon_Crypt_2
SE_23723chr1:202025622-202026632Colon_Crypt_2
SE_23723chr1:202027579-202028063Colon_Crypt_2
SE_24689chr1:202025000-202026731Colon_Crypt_3
SE_24689chr1:202026979-202027324Colon_Crypt_3
SE_24689chr1:202027385-202028078Colon_Crypt_3
SE_26730chr1:202024894-202026849Esophagus
SE_26730chr1:202026891-202028098Esophagus
SE_27624chr1:202025621-202026728Fetal_Intestine
SE_28545chr1:202025609-202026892Fetal_Intestine_Large
SE_31432chr1:202025038-202028197Gastric
SE_33417chr1:202024767-202028250H2171
SE_33792chr1:202025009-202026847HCC1954
SE_33792chr1:202026868-202028524HCC1954
SE_34304chr1:202024742-202028669HCT-116
SE_34741chr1:202024816-202029528HeLa
SE_41626chr1:202025694-202026677LNCaP
SE_43434chr1:202024872-202026814MCF-7
SE_43434chr1:202026895-202028157MCF-7
SE_50066chr1:202024870-202026819Sigmoid_Colon
SE_50066chr1:202026876-202028224Sigmoid_Colon
SE_52354chr1:202025036-202026856Small_Intestine
SE_52354chr1:202027450-202028155Small_Intestine
SE_56834chr1:202025060-202025517VACO_400
SE_56834chr1:202025567-202026651VACO_400
SE_56834chr1:202026926-202027405VACO_400
SE_56834chr1:202027479-202028191VACO_400
SE_57376chr1:202025025-202026652VACO_503
SE_57945chr1:202025717-202026255VACO_9m
SE_65333chr1:202025428-202026806Pancreatic_islets
SE_65333chr1:202027273-202028336Pancreatic_islets
SE_67027chr1:202024767-202028250H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1202025000202025600
Number: 1             
IDChromosomeStartEnd
GH01I202055chr1202024732202028612
Enhancer Sequence
TTCAAGCTGT TCTTCTGCCT CAGCCTCCTG AATAACTGGG ATTACAGGTG TGTGCCACCA 60
TGCCTGGCTA AATTTTGTAT TTTTAGTAGA GTCAGGGTTT TACCATGTTG GCCGGGCTGG 120
TCTTGAATTC CTGACCTCAA GTGATCCTCC CGCCTCGACC TACCAAAGTG CTGGCATTAC 180
AGGTGTGAGC CACCTCACTT GGCCTGATTT CCATGTTTAA AAGCTCACTC TGGTGGCCAT 240
GTGAAGATAG ACAGGAGCAA GAGTGTAGGT GGGACAGCCG TTAAGAGGCT ACTGCAGGCC 300
TCCAGGGTGG AGACAATGGT GCCTTGGACC GGGATGGAGC AGGGGAGGTA GTGAGAAATG 360
GACAGGCTAG GATTATATTT TGGTGGTGGA GCTGAAAGAA TTTGCTGATG AATGAGCTGT 420
GAGGCATAAG AAATACAGGC GGCAACAACA GAGTCCAGGC GTTTGCTGAG AGGATGGTAA 480
TGCAACAGTG AGCACAGGAG GCCAAAACAT CACACTCACA GAAGACCAAT GGTCACTGAG 540
GTTGCTATTT TTTTTTTTTT GAGACAGAGT CTCACTCTGT CGCCCAGGCT GGAGTGCAGT 600
GGTGCAATTT CAGCTCACCG CAACCTCTGC CTCCTGGATT CAAGTGATTC TCCTGCCTCA 660
GCCTCCCAAG TAGCTGGGAT TACAGGCGTG CCCCACCATA CCTGGCTAAT GTTGGTATTT 720
TTAGTAGAGA CAGGGTTTCA CCATTTTGGC CAGGCTGGTC TTAAACTCCT GACCTCAGGT 780
GATCCGCCGA CCTCTGCCTC TCAAAGTGCT GGGATTACAG GCGTGAGCCA CCACGCCTGG 840
CTGCAGTTGC TATTTAGATC TGGAAGGCTT TTCCCAGCTT AGCGTGGTCA AGATAGGGAT 900
GGGCCGAGGC TGGCACTGAT GCTAGACTTC CGTGCACAGG GCAAGTATGG ACAAGCCCCA 960
AGTGGCTTTG TGAGGCCCAC ACAGTGAAGC TTGGGAAATG GGAAGTGGGG CTGCGCCCAG 1020
ATTCTGGTAT CTATGACAAC TAAGGCCGCT GCACATCCTC ATGGCTCTCC CAGAGACCTC 1080
AGGTGAGGCC CTTCTGTGTT CCTCAAGCAC CCATGCCACC TGCGGGGTGG GGCAGGACCC 1140
TCCTACCCAG CCCTGGGCCT CCTGGGGAAC CATGGGTGCA CAGGGGTAAC CTGAGCCAGC 1200
CTCTCTGGGG CATGGGCGGG CGTGGTGGCG TGGGCCTGGC GCCAGAGAGT GGAGCAGAAT 1260
GTCAGCTCTG TGAGCCGCAC CGGGTGCCAG CACTCTGCAA ACAGACTCTA GTCACCAGAT 1320
AGACTGGAGT CACGAACCTA ACAAAGCGCT CAGCTGGGCA ACTGTAACTG CAGAGGGCGG 1380
GGCCGCACAG TGCTGCCTAG TGCCTCCTGC CTTGATCTGG TCAGGGTCAT GGGAGGAGAC 1440
AGGTTCCCCA GGAGGGCCCA TTAACAAGAT TAATTGGGGT GGCCTGGGGG ACTCTGGGAT 1500
GCTCACTGGA AACATATCCT GGGGGAATGA GGTAGGTGGG GAGCCAGGAA AACTGCCCCG 1560
TCTGGTTTCC TTCCCTACAG CCCTTTATCT GGAGAGACAA GCTCTACTAT ACTACAAGGG 1620
GTTAATTTAA GAAGGGGTTG CTGGGCATGG TGGCTCATGC CTGTAATCCC AGCTCTTTGG 1680
GAGGCCGAGG TGGGTGGATC ACTTGAGGTT AGGAGTTTAA AATCAGCCTG GCCAACATGG 1740
TGAAACCCCA TCTCTTCTAA AAAAACAAAA ATTGCCGGGC AAGGTGGCTC ACACCTATAA 1800
TCCCAGCACC CTGGGAGGCC GAGGCGGGTG GATCATCTGA GTTCAGGAGT TCGAGGCCAG 1860
CCTGGCCAAC ATGGTGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC CAGGTATGGT 1920
GGTGCACGTC TGTAATCCCA GCTACTCAGG AGGCTGAGGC ATGAGAATCA CTTGAACCTG 1980
GGAGGCAGAG GTTGCAGTGA GCTGAGATCA CGCCACTGCA CTCCAGCCTG GACAACAGAA 2040
CGAGACTCCA TCTCAAACAA ACAAAACAAC ATCATATTAA AAAGAAAACC CGGGCCTATT 2100
TTTTTTAAAG ACCCACTGCA GAAGTGACCC TTCTCATTGG TGGCTGGTGA AATTGTTCTT 2160
GCCAAGGTTT GGTATGACCA GGTAAAAAGC TTTCAATGCT CAAAGTGAGG AAGCACAGAA 2220
GTCATGTACC CTGCATTGTA GCTGACCAGA AGGTAAATCA AGAACCACTG AGCATGGTTG 2280
GGTGCTGTGG CTCATGTCTG AAACCCTTGC ACTTTGGGAG GCTGAGGCAG GAGGATCGCT 2340
TGAGCCCAGG AATTCGAGAC CAGCCTAGCA ACATAGCGAA ACCCTGTCTG TACAAAAAAA 2400
ACTAAAAAAT TAGCTGGGTG TGGTGGTACA TGCCTGTGAT CCCAGCTACT CAGGAGGCTG 2460
AGGTGGGATG ATCACTTGAG CCTGGGAAGT TGAGGTTGCA GTGAGTCATG CTCACACCAC 2520
TGCACTCCAG GCTGGGCCAC CCTGTCTCAA AAAACAAATA AAAAACAGGA ACCACTGAGC 2580
ATAGGTCACT GGAAGGGAGA TTTTGTCTTA ATAGAAGAAT TCCAACAAGG GGATGGGCAA 2640
TTTTCTGAGA AGGGGACATG GGTGTTTGTT CATGCAAAGC CTGGATGTCA AAGGAACAAA 2700
CAAAGTCTGG GGAACCAACC AATCTCATTG CCAGCTACCA ATGTGGACCA TGCCTGCTGC 2760
AGTTACACCC ACAGTGCTGT AATTCTCAGT CCCTCTGGTC ATCTCTGTTC TCCTACAAGC 2820
CCAAGCCTAC TGTGATGGGG TTTCCTCTCC CTTGATCTAC CCTCCTACTG TCTCCCCACC 2880
CTCCACCAAA CACTCTTCAC TTTCTGGCCT CAGTTAAATT TAGCCCAGCC CTGAGGGTGC 2940
TGCTTCCCTT GGAGCCTGTG TAGCCTGTGA AATCCAGTCA TGCCCTCAGG GGCCAGAGGT 3000
GAGGCAGACT GTCTTCCCTG TCATCTCAGT AACTGTGACT TCCATCTACT AGGTTGCTGT 3060
AACCAAAAAT CAAGATGTCA TCCTTGATTC TTCTGTATCC CTCATTCCTC CTTTTTTTTT 3120
TTTTAAGATG GAGTCTCACT CTATCACCCA GGCTGGAGTG CAGTGACGCG ACCAGAGCTC 3180
ACCACAACCT CCACCTCCCA GGTTCAAATG ATTCTCCTGC CTCAGCCTCC CAAGTAGCGG 3240
GGACAACAGG TGTGTGCCAC CACGCCCAGC TAATTTTTGT 3280