| Tag | Content |
|---|
EnhancerAtlas ID | HS101-39152 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:381240-383110 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_24141 | chr7:380895-383028 | Colon_Crypt_2 | | SE_28128 | chr7:380407-384370 | Fetal_Intestine | | SE_29038 | chr7:379694-384481 | Fetal_Intestine_Large | | SE_31770 | chr7:379498-384580 | Gastric | | SE_47737 | chr7:380239-383352 | Pancreas | | SE_65801 | chr7:378197-384886 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I000340 | chr7 | 380353 | 384367 |
|
Enhancer Sequence | GTCCCCTCAA ATTGTCATCT CTCACCACCC TGGACTCTTC AGGGCAAACC GAGCACTGCT 60
TAATGGAAAC ATTGTTTCTT CAGAGGTGAC AATTCCCCCA CACCAGCGTC GTCTCCAGCC 120
TGGGTAGTCG AAGTGGGGTT CCTGGGCCTG CAGCTCCAGC ATCACAGGGC TCCGCCCCGA 180
CCTCCTAAAT CACAAGACCC TCAGGCGATT CCTGCATTTG ACAATGTGTG AGAAGCACCG 240
GCCTGTGTGG CCAAATCAAC GGACAAATTC TCCCCCGGCA TCCACGCTTG TCCCCCGGCA 300
TCCACGCCTG ACCCTAGTGG TCTTCATCTG GTCCAGAGCT GCCCGAGGAG ACAGGACAGA 360
ATGCAGCAGT AAGGACGACA TTTCCTTCTG CTCACGGGTC CACACCAGGC ATGTTTCTGA 420
CAGCAAGGGT CCCCAGCAGC CCTCAACACT CCAGAGATAC TGGGATCCGG TGTGTAGGTT 480
CCCACTACCC CTGCTCACTT CAATGACTCC AAACTTTTTC TGACCATCAA GCATGTTTTT 540
CTAGAAACCC TGTCTTGCCG GGGCAGGTGT TATCAGCCAC GTCCTGGTCT GTCCTGCAAA 600
AGGAGGAAAT GGCCACGCGC CACCTCCTAG TTCACCTGCA CCTGTGTGGG CAGGTCCCGT 660
GCACCCTGAC TGCTGCCACA CCTGCTGGGG CGTGAGGACT TTCTCGGGCC CCTCGATGTG 720
GCTGTGTGTC CAGCTCCCAG GCACTCAGCG CCCTGTCCCT TGTCCCCTGT CTCCCGCCCC 780
CTTGTTTACC AGTGGGGAAG ACAGGCCTGG CCGGTGGGGG TGTGAGTCTG TCCCTGGCCC 840
CAGCTGTGGA GCAGCTGAGC TCATTGGAAA CCAGGCTGCG GGCCTGAATG CAGCCCTTGT 900
CTCCTGGCCC CTGTTAATAG CCTCTATAAC TGCCCAGCAT TTCTATTGAC TCAAGATAAG 960
TTCCGGGGGC CGGAGAACAG CTCACTGTTT GGCACATGTC TGCTGGCCAG GCCTGGCCAG 1020
ACCGGGATGG CAGGGTTTGG TGAGTCCTGC AGGCCAGGCC CCAGCGGTTG GTGCTGGCAG 1080
CTCAGCAAAC AGCCTGCCCG GGCCACATGT TGCCCTCCTT ATCCCTCGGG CCCCGGCCAG 1140
TAACCTTGCG GCGATTACAC TATCAGCCTC CCTTGGCAGT GCCAGCGTGT GACACACGTC 1200
ACATGTTCTC GAAACTCTGT CCAGAAACAG GTGTTCGAGG TGACATCATA TCTGACCAGA 1260
GATCACTAAG TCTTCCGACT TCTATCAATA TTTGCATTTC CAGCTCCACG GAGAATCTAA 1320
TCAGACTTCT GATGACACCT GCCGTGTTTC TGACCCACTG TGCTCCTGGC TGTGGGTATC 1380
GAGCCCCCGT CTCCACTCAT TTTGGATTTT TACCCTCCTG AGGGCCTAGT GAGCTGACAG 1440
GAAGGGCCTC TGGGGTGGCC AGATGAGGGG AGCAGAGCCA GGGGGTCAGG AAGGAGGCCC 1500
TGGAGCAGGA AGAGGTGGGG TCCAGGCTGC AGGCCTCAGC CTGGGTAGGA AGAGCCCTTG 1560
CTGGGCCCTT GGCCTTTGGT GGCTCTGTCC ACACCTCTCC AGGACAGAAG CTCAACATGC 1620
AGGCCCCAAG CGCAGCGGAA GACCCAGACT CCAATGGCCA AATCAGGCCC AGTCCACAAG 1680
TGCATCCCAG AGGCCGGAGC AGGGCAGCCC TTGGCCACCA GACAAGAGCC AACACTCTGA 1740
ACCACCACGG ATGGGTCCCT GCTCTAGCGG AGGAAACCGC ACCCTTTTTA AAAGAAAGAA 1800
GCAGAAATAA GAAAACAGAG CCCCGTGGCA CCTGCAGGCG GTGGCGTCTC TCAGGCCTCT 1860
GGAGCTCAGG 1870
|
