| Tag | Content |
|---|
EnhancerAtlas ID | HS196-00179 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:10757750-10760680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:10758325-10758335 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:10758325-10758335 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:10758325-10758335 | AATGGAAAAT | - | 6.02 | | PHOX2A | MA0713.1 | chr1:10758383-10758394 | TAATTCAATTA | + | 6.14 | | Phox2b | MA0681.1 | chr1:10758383-10758394 | TAATTCAATTA | + | 6.14 | | RREB1 | MA0073.1 | chr1:10759784-10759804 | CCCCAAACCAAAATCCAACA | + | 6.07 |
|
| | Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
| SE_23439 | chr1:10759150-10759719 | Colon_Crypt_1 | | SE_23439 | chr1:10760159-10760720 | Colon_Crypt_1 | | SE_24212 | chr1:10757813-10758267 | Colon_Crypt_2 | | SE_25175 | chr1:10757709-10758336 | Colon_Crypt_3 | | SE_25175 | chr1:10758675-10759981 | Colon_Crypt_3 | | SE_26713 | chr1:10757605-10758307 | Esophagus | | SE_26713 | chr1:10758560-10761323 | Esophagus | | SE_31374 | chr1:10751200-10758378 | Gastric | | SE_31374 | chr1:10758561-10760925 | Gastric | | SE_40607 | chr1:10741152-10758351 | Left_Ventricle | | SE_40607 | chr1:10758374-10760888 | Left_Ventricle | | SE_41555 | chr1:10757798-10758295 | LNCaP | | SE_41555 | chr1:10758587-10759679 | LNCaP | | SE_41555 | chr1:10760096-10760877 | LNCaP | | SE_42099 | chr1:10754655-10758223 | Lung | | SE_42099 | chr1:10758527-10759897 | Lung | | SE_42099 | chr1:10760066-10760991 | Lung | | SE_47486 | chr1:10757813-10758169 | Pancreas | | SE_47486 | chr1:10758585-10759776 | Pancreas | | SE_49447 | chr1:10758606-10759639 | Right_Ventricle | | SE_65281 | chr1:10755010-10758400 | Pancreatic_islets | | SE_65281 | chr1:10758555-10760711 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 4 | ID | Chromosome | Start | End |
| GH01I010698 | chr1 | 10757664 | 10758631 | | GH01I010702 | chr1 | 10759151 | 10759719 | | GH01I010699 | chr1 | 10759941 | 10760090 | | GH01I010701 | chr1 | 10760181 | 10760330 |
|
Enhancer Sequence | CTGCTCTCAT TTTGAATTTG TAACTTTCAC ATAAACTTGA ACAAAGCTCC TTTTGTTATT 60
GCACCCCACC CCAGGATCCC AATAAACTGG TTCCATCTGA GGCGACTGGG CCAGGGCACA 120
GAAGCCTTGG CCAAAGGACT GCGTGTGCCT GCGAACAAGC ATGTTCGCAC CTGCGAGGGA 180
GTCCGTGTGT TTGCGTGTGA GCCCGCTCCG GGGCCGATGG AGGGAGGGTG TCGGGAAAGC 240
TGTGAGCCAG CGAAGTGGAC GGGAAGCATG GGGGCCGAGG GAGGGCAGAG CCAAGGCACC 300
ACGGCATGGC CACGGGCACG GGAGGTCGTG GGCCACAGAC AGGTGGGTGT TGGGGCAGGG 360
GGTCAACAGG ATGAGAAGGA AACAAAGGGG AGAAAGGAGC CACAGAGTGG GTGGCGGAGC 420
GAGGGCCGCG CCGAGTGTAA GGCAGACGCA GGGATTGCAT TATGGCAGGA GAGGGGCTGG 480
CACAGCCGCA CGCTCGGCCC CGTAATCCTG TTAGCCAGCA ATCTCCATTC CGAAAGAGCT 540
TCATTTCTTT GTGAATATTT GTAAACTAGA TATCTAATGG AAAATTATAG GAAAATTATA 600
GTGAAATTCA TGACGGAGAA ATCCGATTAT CCCTAATTCA ATTATGCCAT CTTAGCCCAC 660
ACAGCACATT TCCCATTTTT TTCCCATAAA TACCGATGCC AGGGGTCCCG GTAATCAAAT 720
AAAATTGAAA ATCATCTTCC CATTAAATTC AATTAGCCGC AATTTCTAAA GCCTATCAGA 780
GATTTTAATT ACTAAATTAT AAAATTCTCC AATGCTAAAT TGAAACCAAA AAAATTGCAC 840
ATCCTTATAT TTCAGAGAAA AAGAAAGGCC AGCAAAATCC TTGAAAAATG CCCTCTTCTC 900
TGTGGCCGGC TCCGAAGCAG GCTCCCCACC TGGAAGAGGC CCACCATCAC TGCCTACTTG 960
TCCAGCTGGG GATGAAGCCA AGGGGCCAAG GAGGGTCCCT GGCAGGGGAG GGCTGAGGGG 1020
GACTGGCTTA ACAGAGGGGC AAGCCGCACC TCCAACCCCA GCGAGCTCCT CCAAACTGGC 1080
CTTCCTCTCG TGGGCTCTCC TGGCTCCTGA GAAGTCCTCA GCTCTGTCTC ATACCAGGAA 1140
GCCTCTAACT CCCAGTGTCA CCTTCTTGGC CCATGAATTG GGCTCAGGCT TAGGTCACAG 1200
CTTGGCCTCA GGGCTCTGTG TGGCTCCAGC ACAGCGGACC GGACCGGAGG CAGCCAGCTC 1260
TTACCCAAGC ACTGGCTCTC CAGCCACTCA GCTCCCCCAC CGCTCCCCCA CCCATGGCCT 1320
GGCCTGGGTT GGGGGTGGGA GCAAGATGGA GCCTGGGGTT GGGGGTGGAC AGGTATCACA 1380
CATGGCTCCA TGGCCCAGAG GCTGCTTGCT CCAGGGCGTT CTCAGGGGCC CATGAGGCCT 1440
GGCAGGGTAC CAGCCTTCGG GGAGAAGAGC TGGGGATCGA CATGGCCCAA ATCTGGCCTC 1500
TCCCTGCACT TCCAGCTCAT CCTCCGTTCT CCTTCCCCTC TCCTGGGAAG TCAACGGCCC 1560
TGAACTGGCC AGGAGGAACG CCCTTGTGCC CTGGGAGAGG ATCACACTTT CCCCCCATTT 1620
CCTTTTAGGG AAGTGCTGGC CACAACCCCA AACAGTAGCC CCTCCTCTTC CCCCAACCCC 1680
CACATCCCAC TTACCCTGCT CTAAAAGGTG CTCTCAGAGT CAGTAGAGCC TGGGGATGTG 1740
GCATCGGTGG GGGCATAAAG TGACCCAAGG TCTGAAAGCC AAGGTAGGTT GTTGGGTGGG 1800
CAGCTGGCAG CCCTGGCAGA TCCAGGACAG TCGGCAGAAG TCTTGCTGGC AGCCCAGCAC 1860
CCAGGGAGCC GGGAGCAGGT TTAATTTGCC AGGCAGCCAG GAGTGCCAGC AGGGGAGGCA 1920
CCCGCAAACA AAACAAAAAC AAAAAAGTTA ATTATCTTTG GCTTTTTCTT AATAAATATC 1980
CAAACTGGCC CGGCCGGATC CTCCACTTTG GAGGGAGAGA GAAGGAGGAA AAAACCCCAA 2040
ACCAAAATCC AACAGACTGA TTCTCTTGTG TCTCCCTTCC CCTTTGTCTC ACCCTTGTAG 2100
GTTTCTCTTA TCAGAAGCAG CGACGGTTTC ACATTAATTT CCCAGTTTTT GTGAGTTCAA 2160
GAGTGTGGCC ACAAAAACTT TAAAAAAAAG TTTTGGGGTG GAAACGTGGA GTGTGAGAGA 2220
AGAGAGAGGT AGGTGGGAAG AAAAAGGTGA GAAGAAACAG AAGAGAAGCA GAGACAGAGA 2280
GAGAGAAAGA GAGACAGGCA GAGAGAGAGA GAGAAACAGA GACAGAGAAA GAGAGAGAGA 2340
GACAGAGAGA GAGAGAAAGA GAGACAGAGA GAGAAAGAGA GATAGAGACA CACACACACA 2400
CACACACACA CACACACACA CACAGAGTAT GAAGCAGGGA CCTGGGCTAG TTGGGTTGCC 2460
CTGTGGGCCT GGCCCAGCCT GTGGCCCCAG CCCGGGCGGG GACCTGTTCT GGAATGTTGG 2520
GTTGGCATTT TGTCTCAGTT ACAATGATCA GCTGCAGAAG ATATGGGATT TCTCATTTTA 2580
AGCTCTGAAA CCACTTAGGT TTCTCTGGCT ACTTCAGTTA CCCTGTTGCT GCTGGTTCCT 2640
GCTCCAAGCC TCCCTTCTAG GAGCAGGGCT GGGGAGAAGC CAAGGGAGGG GTCCCAGGAG 2700
GGGAGGCCCG CTGTCCTTAT GGGAGGTGTG AGGTTTTCTA TGTGGAGCTG CCAGCGTACT 2760
TGGGGAGAAG ACACGTGTGC TGCTGCCTGA GTCTAGGTGT TTGGATGGTG TATGTACACG 2820
CCTGAGCCTG AACTGTCAGA CACACATGAT AGGCACATGT GTGTCAGGGG TGGGGTGGGG 2880
GTTAGCCAGG ACATCAAGCA ATCCCTCATG GAGCACCAGC TCTGGAGTCT 2930
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