| Tag | Content |
|---|
EnhancerAtlas ID | HS048-01633 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:68165960-68167140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:68166534-68166555 | GGGGGAAGGGGCAGAAGAGGA | + | 6.09 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_02387 | chr1:68166569-68167337 | Astrocytes | | SE_27725 | chr1:68165776-68167750 | Fetal_Intestine | | SE_29142 | chr1:68165684-68167885 | Fetal_Intestine_Large | | SE_38054 | chr1:68165922-68167557 | HUVEC | | SE_40089 | chr1:68165860-68167362 | K562 | | SE_41280 | chr1:68165990-68167378 | Left_Ventricle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I067700 | chr1 | 68165730 | 68167787 |
|
Enhancer Sequence | GAGCCCCAAA TAAAAAGGTT TAGAGGGAAT ATCCATGTGT TTATGTGTAA CTGACCCTCG 60
TGCCAGGGAA AAACTGATCA TGGCACATAT CCAGAAGAGG TGGAAAGCCC CATGACATGC 120
ATCTCCACAC TGAGTTCCAA TCACTACCCG CAGGCCTGGG TTTCTTGTCC ATGTTAAGGC 180
TAAGTATACA TCTCATCTGC CTCTTCCAGC TTCATTACCT TCCCTTCCCC CATCTTTTAA 240
AAACTCACCC CTACCCAATC CCATCCATCA TCCCCAACTC TCCTCCACTG AGAGTTACAA 300
GAACTTTGTA ATTTGGTCAG AAGCAGTAAA AAGTGCTTGT TAGTTGTTGC CTCTTTTTCA 360
AAACCGATGT ATCTAAATCC TTCAGTCTTT TACTAGAAAG GGCCCAGGGA CTGTCTTTTG 420
CCCCTACCTT TTGTAAGTGT GGAGTGCTGG CTCTCAGAAG CAGGGGCCAT CTCTGCAGCG 480
TGTCCGGTTC ATAGCCTGGG GCTTGTTGGC TGCCTCCCGC CCTTGTTCTT TGATGATTTT 540
GCCCTCCCCT CATCTCTGTG GGAATCCCAG CCCTGGGGGA AGGGGCAGAA GAGGAGGCAG 600
GGCACCTTCA GCAAACACAT AGTGAATATG AGTCACCACC ATCTAATGAC CTTTCCATTT 660
GTTATCAGTT TCCACTACCT CAGCTAGTCT CAGGATGGGA AACAGCCCTC CACAGGTCAG 720
AGTCATTACG TCACTCCTCA GCAGCCTCTC TAGCTCCCCT GTTGGTTTCA GGATAGGCAA 780
GCAGGATAGG AGGGCGGGAT CGGGGGTCTT CTGCACACTG GCTTCCAGTC CTCTTTTCTC 840
CTCCTCTCAT CTCCTCCCAG GACCTCATTC CAACGCATAC TGTTCTTCTC TCACTCAGCC 900
CAAACATCAC CACCCTTGGA AGCCTTTTTA GAGGTCTTTG TTGATGTGGA GCTAGTCCCT 960
CTTTCCTCTG GGCTCTCACA GCACTCTGTG TTCACCTGAG TTATAGCACT TGCCACATGA 1020
TACTACGATG ATTAGTTTAC ATATCTGTCA TTCCCATCCT CCTTGCTCAG ACTGTGACAT 1080
GGGCTGGTGT AAGTCTTATT CATTTGGGTG TCATGGGAGC CTGACTCTCA GCAGCTTGCT 1140
CTCAGGAGGT GCTCAGAAAA TGTTAACTGA GTGAAGGAAG 1180
|
