| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00062 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:1984630-1985390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:1985144-1985159 | AGAGGTCAAAGGTGA | + | 6.8 | | Nr2f6 | MA0677.1 | chr1:1985145-1985159 | GAGGTCAAAGGTGA | + | 6.59 | | Rxra | MA0512.2 | chr1:1985145-1985159 | GAGGTCAAAGGTGA | + | 6.65 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28368 | chr1:1981806-1986083 | Fetal_Intestine | | SE_29491 | chr1:1981921-1986311 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CGAGGTTCAA GCAATTCTCC TGCTTCAGCC TCCCTAGTAT CTAGGACTAC AGACGCCCGC 60
CACCACGCCC GGTTAACTTT TGTAGTTTTA GTAGAGATGA GGTTTCACTT TGTTGGCCAG 120
GCTGGTCTCG AACTTCTGAC CTCGTGATCC GCCCGCCTTG GCCTCCCAAA GCGCTGGGAT 180
GAAAGGCGTG AGTCACCGCG CCTGGCCCAG CTCAGACAAC GTTTGTGTTC AGGGAGCTTC 240
TGTGTGCAAA GCCCAGGGCT TGGTGCTGAG GCCAACAGAG ACGCAGGAGT CTCTCCCGGG 300
CGGCCCAGCT GGCTGCTGGG TGCTGAGTCC TGGACGCCCC TGCTGAAGGG CACAGGGCAG 360
CTGTTTGATT CAGGATTGGG ATAGGGTTGG AGGTGGTGGC CTGACACTTC CCAAGCCCTG 420
GGGTTTTACT GGAGCCACCC ACCTGGCCTC TAGATTGGCC GGAAACTGGC TTCCACTGGA 480
GGCAGGACTG TAGGGGTAGG GGCGTGGGGC AGGAAGAGGT CAAAGGTGAA GTGATGGCCG 540
ACTCCCACTC TGGAGTTCCT GGTGGTCAGA CTTTTGGACT CCAGGTCAGG CAGCAGGCGT 600
GGATGTCAGC TTGGGGCGAC CCCAGGGTGA TGGGTGTGTG ACCCCCCTCC ATTCCTTACT 660
TTCCTAATCT GCCATGATGC TGTGGGCTGT GGCGAAGACC AGCCAGGTTG GTTCCTGTGG 720
GGTGCTTGGG CACTGGGGGC AGGTGCTGGG TGGCCAGTTC 760
|
