Tag | Content |
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EnhancerAtlas ID | HS102-14897 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr21:40158920-40161300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx3-2 | MA0122.3 | chr21:40160831-40160844 | TTTAAGTGTTTTT | - | 6.64 | ONECUT1 | MA0679.1 | chr21:40159534-40159548 | CATATTGATTTTTT | - | 6.29 | ONECUT2 | MA0756.1 | chr21:40159534-40159548 | CATATTGATTTTTT | - | 6.25 | ONECUT3 | MA0757.1 | chr21:40159534-40159548 | CATATTGATTTTTT | - | 6.58 | PLAG1 | MA0163.1 | chr21:40159506-40159520 | CCCCTCTGGGCCCC | - | 6.36 | PLAG1 | MA0163.1 | chr21:40160484-40160498 | GAGGCCCTCGGGGG | + | 6.62 | POU4F2 | MA0683.1 | chr21:40161097-40161113 | CTTATTAATTATGCTT | - | 6.56 | RREB1 | MA0073.1 | chr21:40159442-40159462 | CCCCCACCCACCCCCACCCG | + | 8.75 | ZNF263 | MA0528.1 | chr21:40161252-40161273 | GGAGAAGGGAGGGGAGAGGGC | + | 6.54 | ZNF263 | MA0528.1 | chr21:40161246-40161267 | GAGGGAGGAGAAGGGAGGGGA | + | 7.52 | ZNF263 | MA0528.1 | chr21:40161249-40161270 | GGAGGAGAAGGGAGGGGAGAG | + | 8.04 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_23299 | chr21:40159082-40160667 | Colon_Crypt_1 | SE_23922 | chr21:40159153-40160245 | Colon_Crypt_2 | SE_23922 | chr21:40160251-40160569 | Colon_Crypt_2 | SE_24852 | chr21:40159099-40159661 | Colon_Crypt_3 | SE_24852 | chr21:40159665-40160215 | Colon_Crypt_3 | SE_24852 | chr21:40160856-40162402 | Colon_Crypt_3 | SE_25850 | chr21:40157795-40162661 | Duodenum_Smooth_Muscle | SE_26886 | chr21:40159374-40160355 | Esophagus | SE_27636 | chr21:40156196-40163184 | Fetal_Intestine | SE_28570 | chr21:40157745-40163071 | Fetal_Intestine_Large | SE_34978 | chr21:40159039-40160957 | HeLa | SE_36155 | chr21:40158929-40160950 | HMEC | SE_47242 | chr21:40156323-40162674 | Panc1 | SE_50186 | chr21:40159118-40160754 | Sigmoid_Colon | SE_50186 | chr21:40160865-40162903 | Sigmoid_Colon | SE_52374 | chr21:40159046-40160821 | Small_Intestine | SE_52374 | chr21:40160960-40163050 | Small_Intestine | SE_56279 | chr21:40158914-40160830 | u87 | SE_56782 | chr21:40159078-40160845 | VACO_400 | SE_56782 | chr21:40161059-40162354 | VACO_400 | SE_57400 | chr21:40159137-40159496 | VACO_503 | SE_57400 | chr21:40159656-40160695 | VACO_503 | SE_64260 | chr21:40158863-40160711 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I038784 | chr21 | 40156288 | 40163267 |
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Enhancer Sequence | GATCAATTAA AGAGTTGAAC ATTTGAAAAG AAGAAACATG AAAATGAATT TCTAACTGTA 60 CGGTATTGAA TACATGAAAG TTCTCTTAAA CTTAGTCCAG AGTCTCAATA AACATGGTAA 120 GTATGTAATA ATTCACATTT ACAACCGCCA TAAAAACTCT ATCAACCAAA TTATTTTATG 180 ACGTCAAAAT TATCTGAAAA AAATTGAGGA ACTAAAATTT TTAAAAATAG GTTCTCAGTT 240 AGAGCTGTCT ATTAAAAGGA TAAATTTTAA ACTCTCCGGA GCTGGCCTTC CTGGTTCCAG 300 GAGCAGCCTG TTGGCCTTCT CTCGCAAAGC TCAGTTCCTT TCCTCCATTC CAGAAGACCC 360 TCAAGCCTGT CCCATGCACC TGGTTTTACA TTTTTAAATG TTAAAAGGAA GACCACCGTG 420 AAAGATTGGC ATGTTAATAG TAGGCTAAGG CGACAGGTGC TGGGGCTCCG GCTTAGAGAT 480 CCCCACAGAT TCCATGCTCC CAGGGCTGGC TGCAGCCATC TGCCCCCACC CACCCCCACC 540 CGGCCCAGCC CTCCCCTCCT GGAGGTGGAA TCGTGGCTTG CACAATCCCC TCTGGGCCCC 600 TGGGGGAGGC GCACCATATT GATTTTTTGG ACTTCGTTTC TGTGTGTCTC ACCAGTCTTT 660 GCCCGGCACA GTGACTCACT GGCGTCCCTT TCAGGACTTT CTCCCGCCTG ATAACATCTA 720 AATGACTCAT GCCTACACCA CCTGGAGAGC TCAGGGAAGG CACGGTTTGT TCAGGCCACC 780 CTCACTCCAA GGGCCAGCCC TTTTTTGGAA TAGAAACTAA AAGTTGGTAG CTTCCATTTG 840 TAGTTCCATC TAACAGAAGA GCCGACCCAC TCACATTAGC TGGCTCACGA CTAAGGCAAC 900 CAATGCCTCC CAGAACATAG ACTCAACTGG CAACCCCGGC ACTGAAGGTC AAGGTGAGTC 960 AAAGACACTC ATGCAGAAGG GTGGATGCTC TTCCAAGTGT GACTGGCTGG CCTGCACGGC 1020 TCACTGCCTC CCCTCCTCCC GTCAAGATGC AGCTTCAGTT TAAACCACCT TCGTTCCATT 1080 CATCAAAGAG GAATATTTAC TGTTATTGTA ATGACTCTTC TCACAGTACA CAAGGCTACA 1140 CCTGAAACAC ACAGGCCTTT CAGAAAGCAC AAAGGAGCAT TGTGCAAGCC CCTGCCCAGT 1200 GAGATGGATG GGGGCGTAGA CACGCCAGTT AACAGCCGGG CTTTGCAGGC CAGCAAGACT 1260 TATCTGTGGC CGCACCATGG CCACTGAGCT TGTACCTTTC TTCTTTTAAA AATTGCTCCT 1320 TCATTATAAG CAGAGTTAAA TACCTGCACA TGTGATTTGT GTTGAAATAA TAAAGCAACA 1380 AACACACATC AAGCTGAGGA GAGAATCTTG GCTAAGGTAG GAAGTCGTGG GTCTGGTCTC 1440 AGTCTGTGCT GCTGACCAAC TGTAAGAACT CAGAACTCAC TGTCCACTCA GGACCACAGT 1500 GTCTCATCTG AAAGGACGAG GAGACTGGAA CACACCAGAG CCATGGTTCT CAATGTGTGG 1560 TCCAGAGGCC CTCGGGGGTC CCTGAGCCTC TTTCTGGGGA TCTGTGAGGT CAAAACTACT 1620 TTCACAAGTA TGGTTTGCCT TTTTCACTCT CACTCTCTCA TGCTTGAACA ATGGAATCTT 1680 CTAAAGGCTT CCTGACACGT GATGCTACAA TGGATGGAAT CCAGAGGTGG ATAGGAGAAG 1740 CCAGCTGCCT TCTATTAAAC CAGAAATGAA GAACATTTGC AGAAATGTAC AACAATGCCA 1800 TGCTTCCCAT TAATTATTTT GTTCTTGCTT TAGAATATGT CACTTTTCAT TGAAAAATGT 1860 TACTCATGAT TTTATGTAAA AGGTTTATTG TTGTTACTTT TAAATACATA TTTTAAGTGT 1920 TTTTTAGTTT TGATTTCTAA TATGGCAAAA ATTGGTAAAA TCACATACAC AAGGGCTTTT 1980 GGGGATCCTC AAAACTTTTT AAGAGTGTAA AGGGATCCAG AGACCAAAAG TTTGATAACC 2040 ACTAACCAAA AACTTTGACA ACCATCATCT TGAAGGGTCC TTGGACTTTC TGGAATTTGG 2100 ATCTCCCTTG CCTTGTTCAG TTTTCTCTCT TTTTAGCCAT CTCGTACTTA CTGCCATTTC 2160 AGTTCCTATG TACCTGACTT ATTAATTATG CTTATTGTTT ACCATGTGTG TTCCCCTCCC 2220 ATATAAACTC CATGAGGACT GAGATATTTG TCCATGATGT TCATCAGTGC ATCCCAGGCT 2280 GCCTAGAACT GGGCCTGGCC CTTAGCAGGC ACTTGTTTTT GGATGGGAGG GAGGAGAAGG 2340 GAGGGGAGAG GGCAAGTTCT TTCAGTGTCT GTATAATGGA 2380
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