| Tag | Content |
|---|
EnhancerAtlas ID | HS048-10347 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr13:43555480-43556880 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28291 | chr13:43555351-43556209 | Fetal_Intestine | | SE_29050 | chr13:43553744-43557463 | Fetal_Intestine_Large | | SE_59997 | chr13:43543432-43575380 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 43555480 | 43555882 | | chr13 | 43555990 | 43556545 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I042980 | chr13 | 43554589 | 43557373 |
|
Enhancer Sequence | TAATTGAACT AAGTTTCTTT CTCATTTCTG CTATGGTTCT ACTGATTATT GTTAGTAATA 60
TGTTTTCAAG CTTTCATCAT CCTGTTGATT TATTGTTTCA CCGTTCCAGC TGCCAAAGAC 120
TTTTTAGCAA TTCCCATTCA TTTTTGGTGA TATTGTATTT GAACAAAAAT GATTGCTCCC 180
CAAGGCTTGG CAGACCACAA ATGCGTACCA TACTGAGGAA TGGAATCCAG TGCAGAAAAG 240
TTGGAAATTC CTTCTAAACA GGACCATAAT TTCTACCGTC CTGCACAAAC AGGAATGTAA 300
ATTTGATCTA ATCAAACCAA AATGTTTTTT TCTTTTCATC CACTCTGTCT CTTCTGCCAT 360
GCATAGAACT GTGCTTTTCA AACTGTAGGA GGTAACCCTC TAATGGGTTA TGAAATCAAT 420
TCAGTGGATT TATTTTTAAT GAACAAGAAT AGAAACTGTC AGAGTACATC ACATATAATA 480
AAGGTGAAAA TTGTTTTGTG AAATTTTTTC AGTTATATAT ACCCTAATAT ATACTCAGTC 540
AGGTACTAGG TCATGATGTC AAATGAATTG CTCACTGCAG GCTATGATCA GAAGTCTGAA 600
AAAAAAATCA CTGTAAGTTA CTATGTTGTT GAGGTTGCAC AGTGAGAGTG AGATAACTGC 660
TCTAATGTCA GAGGTGTTTG AACCAGAGAG ATTCCACCTT GAATAGGGGC TGGGTAAAAT 720
AAAGCTAAAA CCTGCTGGGC TGCATTCCCA GACAGTTAAG GCATTCTAAG TCACAGGATG 780
AGATAGGAGG TTGGCACAAG ATACAGGTCC TAAAGACCTT GCTGATAAGA CAGTTTTCAG 840
TAAAGAAGCC AGCTAAAACC CACCAAAACC AAGATGGCAA CGAGAGTGAC CTCTGGTTTT 900
CCTCAAAGCT ACACTCCCAC CAGCACCATG ACAGTTTACA AATGCCATGG CAACATCAGG 960
AAGTTACCCT AGATGGTCTA AAGAGGGGAA GCATGAATAA CCCACCCCTT GTTTAGCATA 1020
AAATTAAGAA ATAACCATAA AAATGGGCAA CCAGCAAGCC TTGGGGCTGC TCTGCCTATG 1080
GAGTAGTCAC TCTTTATTCC TTTACTTTCT TAATAAACTT GCTCTCACTT TGCTCTATAG 1140
ACTTGCCCTG AATTATTTCT TGTGTAACAT CCAAGAACCT TCTCTTGGGG TCCGGATCAG 1200
GACCCCTTGC CAGTAACACT AACACAAGGC TACCAAGCTC ACCTGTCATT TGTGAAAAGC 1260
AGCAGAACAA AGGGAATCCC CAGAGAAACT TTTCTCCTGC AAAGTACTTC TCTATTCAAA 1320
TCATTTTAAA GCTATGATGG GGTTCACGAC ATGTTATCCC AAAATATAGC ACCTTGGTAT 1380
TTGAGAAAAC AGCAAAAGGA 1400
|
