| Tag | Content |
|---|
EnhancerAtlas ID | HS180-36279 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr4:40527740-40528850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr4:40527874-40527886 | TGCCCTGGGGCT | - | 6.11 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_00997 | chr4:40527690-40529323 | Adrenal_Gland | | SE_09152 | chr4:40527205-40528858 | CD14 | | SE_27851 | chr4:40527157-40529140 | Fetal_Intestine | | SE_28685 | chr4:40526940-40529352 | Fetal_Intestine_Large | | SE_31512 | chr4:40527049-40529235 | Gastric |
|
| | 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 |
| GH04I040524 | chr4 | 40526490 | 40529332 |
|
Enhancer Sequence | AGGCTTGGTA AAAACCTAGG GAATAGGCTT AAGTAGAAAG GAGATTTGGG AAGCTCCAGG 60
GCCCTTGGAC ACCTGGCAGT GAGCATCAGA AAGAAAAGTA AGAGTTCTTA AGAAAAACCA 120
ATCAACTTTG CATTTGCCCT GGGGCTGGCC TGGCAGTGCT GCTATCAGAA TTCAGATACT 180
GGCCCAGCCC TGCTCTAGGG CCTGAAGTTT GGCTCTTGCC TCTTCATTTC AGTCCCTTTA 240
GCTGCCCATC CAATCTAGAT CCCCGGAGTG CTCAAAGGAG AGGCAACAAG AAGAAAAAGA 300
AAAAGAAGGA CAAACTGAAA TGCAAGCATG GACCTTAGAT GACGATTCTC ACAGCTCTCC 360
CCCTTCATGG GACCTTCAGA ATTCATTCTT GTGAAAGCTG TAAGTCAAGG AGGACACAGC 420
CAGAAACCGT GACTCATCAA ATTCCCAAAG CCAAGACCAG AACACACAGA CTCTGGATCC 480
AAGGACTCGC TTTCTGCTTT CAGAACACGG GATCCTGCCT ACTTTGTAGT ATTTCAATAC 540
AAAGCTGATC AAGCCGAGGG TCCCCATCTA CTCCCCGCCA GCCTGGCTGC CCTTCCCTGT 600
CTTCAGAGTT TTCTAAATCA TAGAGAAGAT AGAGTTTAAT TCCATGGTGT TTGAGTCACA 660
GGACCTTAGA ACACTTCAGA AAACGATTGG CCTTAAAAAA TGGTTGGGTC TGTACAAGAA 720
AGTCACTGAG TACAGAGGAT GGCAAACATT TCTGTCATGG GCTAGGTAAA TACTATAGGC 780
TTTGCAAGCC ATGTGTTTTC TGTTACATAT TATTCTTTTA TTTGTTTCTT TTTGTTTTTT 840
GTTTTTGGGG TTTTTGTTTT TTGTTTTTGA GACAGGATCT CCCTCTGTCA CCCAGGCTGG 900
AGTACAGTGG TGCCATAACA GCTCACTGCA GCCTCAACCT CCCTGGCTCC AGGGATCCTC 960
CTGCTTCGGC CTCCTGAGTA GACTGCAGGT GTGCTTCACT ACACTTGGCT AATTTTTTTA 1020
TTTTATGTAG AGACAGGGTC TCTCACTGTG CTGCCCAGTT TGGTTCTTTT TTTTTTTTTT 1080
TTTTTTTTTT TTTTGCAACC TTTTAAAAAT 1110
|
