Tag | Content |
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EnhancerAtlas ID | HS007-01249 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:204268590-204269820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA(var.2) | MA0730.1 | chr1:204269129-204269146 | TGACCTAGAGATGACCC | - | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_28816 | chr1:204267256-204269628 | Fetal_Intestine_Large | SE_31690 | chr1:204268354-204268772 | Gastric | SE_37243 | chr1:204260462-204271182 | HSMMtube | SE_65374 | chr1:204268084-204269059 | Pancreatic_islets |
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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: 3 | ID | Chromosome | Start | End |
GH01I204298 | chr1 | 204268085 | 204269059 | GH01I204299 | chr1 | 204269081 | 204269230 | GH01I204300 | chr1 | 204269439 | 204272341 |
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Enhancer Sequence | ATATAGGTGA GCTAAGGTCC ATAGGGAAGG TGGCAGGGGA GGACTGCTGA CCGAAGGACT 60 CAGGGAGCTC TGAGCCGGCA GCCAGCAAGC TGACACAGCT TTGAGACATT TTCCCAGAGG 120 ACAGCCATTA TTGAGGGGAG AAAACATCTC GCATTCTTTC TCCTGCACTT TCCAAAGCAA 180 CGTGGGTCTT CTACTGTCTT AGGGCCTCAC AGTTCTCTCA GGCTAAGAGG TTTAACCTGC 240 CCCCTCATGT CTTCTTTAGA AAGGCCTACT TCCCTGGCAC CAATTCCATG AGCTAATGTC 300 CCCTTTAAGA ATATTTTTTG CCCCATCTGT TCTCTAGTTG GCTGGAGCAG ATGTTCTTTG 360 TTCCTGTGGA AACTAACCTA CCACCCTTCC TAATGGGTGT CTCCCTAGTG AAGCACAGGC 420 CACTCCCCTG CCAGAGCAGC CGGCCCTTCT ACTGCTTGGA GTTCACTGAT GGCAGGCTCC 480 TCACCACAGA GGAACACCAT GGACACATGT GCCTGAATAT TAAGAGTCCA GATCTTGCCT 540 GACCTAGAGA TGACCCAGAA ATGGCAGCCG CCATCTGACA GTACTTAGAA GATAGAAGAG 600 GGAGGTTATC TATGCCATTG CCCAGACAAC AGACCAGGGT CCATCTTTCC AATGATGTGT 660 TAACAGCAGG GTGCATCTTC AGCAGATTGA ATTAGTGCTT CCTTTGACTG TTTTTTCATA 720 TCACTAATGA AGACCAGAGA GACTCCCTAA TTGAATTCTC CCTATTTCAA GCTGCTCATC 780 ACTCTCAAGC TTACCCAGGG CTCATGATCC TTGAGGACAA TCCTTCTCTC AAGACAGGTC 840 CCCACTCAAG GGAACACTTC TCCAGCCATG CAATGCGTGG GGAAGCAGGA AGCACTGTGC 900 ATTTCACTGG CTCTGTATGG GGGTTTCTTC CACTGCAGAT AATGCATCTC TCACTAAATC 960 CAACTTGACC CCATTTGTTC TTGGCTCTCA TAGCCCCGAC AAAGCCAGCT GGATTCTTCT 1020 TGTAAGCCAC AAAGTTGACT GAAATTTAGC TTCCTCTCTT CTGAGCCATT AGCCTACTGG 1080 GATCCCAGAA GTCAATGTAT AAATAAGAAC AAGCCAATAA ATGATCCCTA TCAGATGTCC 1140 AGAAAGTACC CCCCTAATCA GAGAAGATGT CAAAGTCAGA GCTCCCCGTG CCCACCCTTG 1200 AGTTGTCTTC ATTCATTCTA AAGAGGTATT 1230
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