| Tag | Content |
|---|
EnhancerAtlas ID | HS101-03626 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:201990580-201993500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:201991522-201991537 | GAGGTCAGAAGTTCA | + | 6.38 | | TBX21 | MA0690.1 | chr1:201992769-201992779 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr1:201992769-201992780 | AAGGTGTGAAT | + | 6.02 | | ZNF263 | MA0528.1 | chr1:201992213-201992234 | CGCTCCTCCTCCTCCTCCTTC | - | 8.44 | | ZNF263 | MA0528.1 | chr1:201992216-201992237 | TCCTCCTCCTCCTCCTTCTTC | - | 8.69 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_23058 | chr1:201990827-201991297 | Colon_Crypt_1 | | SE_23058 | chr1:201991682-201993038 | Colon_Crypt_1 | | SE_23723 | chr1:201990919-201991273 | Colon_Crypt_2 | | SE_23723 | chr1:201991793-201992845 | Colon_Crypt_2 | | SE_24689 | chr1:201990748-201991252 | Colon_Crypt_3 | | SE_24689 | chr1:201991746-201993176 | Colon_Crypt_3 | | SE_25977 | chr1:201991449-201992586 | Duodenum_Smooth_Muscle | | SE_26730 | chr1:201991584-201993071 | Esophagus | | SE_27624 | chr1:201991445-201993333 | Fetal_Intestine | | SE_28545 | chr1:201991443-201993383 | Fetal_Intestine_Large | | SE_31432 | chr1:201991670-201993044 | Gastric | | SE_33417 | chr1:201991427-201994657 | H2171 | | SE_33792 | chr1:201990657-201991281 | HCC1954 | | SE_33792 | chr1:201991430-201993180 | HCC1954 | | SE_34304 | chr1:201991505-201993289 | HCT-116 | | SE_34741 | chr1:201990653-201993194 | HeLa | | SE_41626 | chr1:201991969-201992570 | LNCaP | | SE_43434 | chr1:201990679-201991267 | MCF-7 | | SE_43434 | chr1:201991624-201993665 | MCF-7 | | SE_50066 | chr1:201991627-201993065 | Sigmoid_Colon | | SE_52354 | chr1:201991432-201993050 | Small_Intestine | | SE_56834 | chr1:201991684-201992300 | VACO_400 | | SE_56834 | chr1:201992323-201993032 | VACO_400 | | SE_56834 | chr1:201993070-201993423 | VACO_400 | | SE_57376 | chr1:201991848-201992311 | VACO_503 | | SE_57945 | chr1:201991851-201992344 | VACO_9m | | SE_65333 | chr1:201992691-201993394 | Pancreatic_islets | | SE_67013 | chr1:201991427-201994657 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 201990800 | 201992971 | | chr1 | 201991192 | 201991253 |
|
Enhancer Sequence | GATCACCTGA GGTCGGGAGT TCGAGACCAG CCTGACCAAC ATGGAAAAAC CCTGTCTCTA 60
CTAAAAACAC AAAATTACCC AGGCGTCGTG GTGCATACCT GTAGTCCCAG CTACTTGGGA 120
GGCTGAGGCA GGAGAATCGC TTGAACCTGG GAGGCAGAGG TTGCAATGAG CCGAGATCAC 180
GCCATTGCAC TCCACCTGGG CAACGAGAGC GAAATTCCGT CTCAAAAAAA AAAAAAAAAA 240
TTTACTCCCT ACATCATAAC TACCAGTGAT TTGTAGGACA GAGCACTCAA TGTAGAACAC 300
TCTTCACTTT GCAGATGAGG AAACTGAAGC TCAGAAAAGA AAGGTAACTT GCTCAAAGTC 360
ACAAATCATG TTGAATGGAG CCTGAGCTTC ATGTTGACAG CTGACCGCTT ACTGAGTATC 420
TACTAGGTGC CAGGCAATGT GTCAAGTTAT TGCTTTACAT ACATCATTCA TTCTCTCTGT 480
GTTCATTAAC TGTCTGCTGT GTGCATGGCT CCATGCTGTG TGCAGAAGAC CCAGTAGGGA 540
AGAGGTCACC CAGGGGGAGT AGGAAGCCTA GGCTATGGCC TGGCACGGTG GCTTATACCT 600
GTAATCCCAG CACTTTGGGA GGCTGAGGCG GGTAAATCAC CTGAGGGCAG GAATTTGAGA 660
CCAGCCTGGC CAACATGGCG AAACCCCATC TCTAGTAAAA ATACAAAAAT TAGCCGGGCG 720
TGGTGGCGGG TGCCTGTAAT CCCAGCTACT TTGGAGGCTG AGGCAGGAGA ATCACTTGAA 780
CCCGAGAGGA GAAGGTTGCG GTGAGCCGAG ATCACACCAC TGCACTCCAG CCAGGCGACA 840
GAGTGAGATT CCATCTCAAA AAAAAAAAAA AAAAAAAATT CCTGGTGCAG TGGCTCAGGC 900
TTGTAATCCC AGCACTTTGG GAGGCTGAGG CGGATGAATC ATGAGGTCAG AAGTTCAAAA 960
CCAGCCTGGC CAAGATGGTG AAACCGCGTC TCTACTAAAA ATACAAAAAA ATTAGCCGGG 1020
TATGGTGGCA GCTGCCTGTA ATACCAGCTA CTCGGAAGGC TGAGGCAGAT AATTGCTTGA 1080
ACCTGGGAGG CAGAGGTTGC AGTGAGCTGA GATCATGCCA CTGCACTCCA GACTGGGTGG 1140
CAGAGTGAGA CTCCATCTCA AAAAAAAAGA AAAGAAAAGA AAGAAAGCCT AGGCTAGAGC 1200
CTAGGAAATT CCAAAGACAT CTATATAAAC CTCTCAACAA GGTAGAGGAT AAGTGCCTCA 1260
TTTCACAGAT GAGCAAACTG AGGCTTCAGA GAGGTTAAGA AAAGCTTAAG CTCTCAGAGA 1320
TAGTAGTAAG TTTAGGAAAC CGGAGCTTGA ACCCTGCCTT CTTTCTTCAA TTCCACAGCT 1380
GACTCTGCTT TGAGAGGTGC TGAGCAACAC AAATGTCTCC GCTGTATGGG TGCCTAAAAC 1440
CCCACCATTA GATGTGCAGT TTGAGGAATG CCCTATGGAT ATACAAACAT GCCTGGGGTG 1500
GAGGGTGGAT TCAATGAGCA TTGCTTTCCA GGGACCCTTG GATCCTGCAG GGTGGATGGA 1560
AAGTGAGTTT TCAGTTCTTC AGAACCTCAC AGTGGCCAAC CCTTGGGAGC ATTGCCCTCT 1620
CATTCTTATC CTACGCTCCT CCTCCTCCTC CTTCTTCTGC TACGTGCAGG GCTGGGCTGG 1680
GGCACCAGCA GCAGCAATTA GCCCAGCTCA GCCGCCCGTT ACTGGAACCT GCATGTCAAC 1740
TCTGGAGCTG ATCCAAGAAA CCACACCCAG TGTCCTGCAT GACTCAACCT CACCTGCCCC 1800
CTCCACACCT GCCAGCCTCA GTGACCCAGG CCATAGTGCC CAGGGGAAAG TCCCAGCATC 1860
CTTTGGTCAA TCCTCATCTA CTCCATGTGT TTGTAAGGCC AGCTGGGATT TAGAGTCTTT 1920
GTATCACAGG CTTGATTCCG GGCTGATTTC TAGCCAGGAG AGAATGCTCC AGGCGGAGCA 1980
AATGCTGGGG TTTGGAAAAC TAGACTCTCC ATGGCAAATG CAGACAGATG GACCTCCTCT 2040
TCACTATCAT TGCTTGAAAC ACGAACAGCT TAAGGCCATG GGAGATATTA CTTTTCATAT 2100
GTCAAATTGG CAAAGAATTA AAGAATGCCC CTGATGTCTA GAGCTGGTGA GGATGTGAAG 2160
AAACTCAAAC TTGACAAAAA CCACTCGTCA AGGTGTGAAT TGAGAGACAC TTTTTTTTCG 2220
AGATGGAGTC TTGCGCTGTC GCCCACGCTG GAGTGTAGTG GTGCAATCTC AGCTCACTGC 2280
AACCTCTGCC TTCCAGATTC AAGCAGTGCT CCTGCCTCAG CCTCCCCAGT AGCTGGGACT 2340
ACAGGCACAC CACCACGCCC GGCTAATCCG CTTGCCTTGG CCTCCCAAAG TGCTGGGATT 2400
ACAGGCATGA GCCACAGTGC CTGGCCGAGA GACATTTTCT TTCTTTTTAA TTTTTTAATG 2460
TTTATTTTTA TATATTTTTA AACTTTTTTT TTTTTTGAGA TAGGGTCTTA CTCTATCACC 2520
TAGGCTGGAG TGCAGTGGCA TGATCATGGC TCACTGTAGC CTTGAGCCTC CCCCACCCCC 2580
AGGGCCCAAG TGATCCTCCC ATCTCAGCCT CCCAAGTAGT TGGGACCGCA GTCATGTGCC 2640
ACCGCACCCA GCTAATTTTT TAATTTAATT TTATTTTTGT AGAGACAGGA GTCTCACTGT 2700
GTTGCCCAGG CTGGTCTTGA ACTCCTGAAC TCAAGCTATC CTGCCTTAGC CTACCAAAGT 2760
GTGGGGACTA CAGGTGTGAG CGGGATATGC TTTCTAAAGA ACTATTTCAC AGATTGTTTA 2820
AAAGCCTTAA AAAACATGCA TATGTCTTTA CACAGCAATT TCATGTCTAA GAATTTTTCC 2880
AAGAAAAATA ATTGGAAAAG TGCACAAAGA TATATGTACA 2920
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