| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04805 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:229199730-229200850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr1:229200027-229200043 | ATTTCCTAGAAGGCAA | - | 6.09 | | BCL6B | MA0731.1 | chr1:229200025-229200042 | TGATTTCCTAGAAGGCA | - | 6.99 | | FOS | MA0476.1 | chr1:229200266-229200277 | AATGAGTCAGA | - | 6.32 | | FOXC1 | MA0032.2 | chr1:229200116-229200127 | ATATTTACTTA | - | 6.14 | | Klf1 | MA0493.1 | chr1:229200448-229200459 | AGGGTGTGGCC | - | 6.32 | | SOX10 | MA0442.2 | chr1:229199835-229199846 | TGCTTTGTTTT | - | 6.02 | | Stat4 | MA0518.1 | chr1:229200025-229200039 | TGATTTCCTAGAAG | - | 6.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_49843 | chr1:229199865-229200817 | RPMI-8402 |
|
| | 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 |
| GH01I229064 | chr1 | 229199880 | 229200783 |
|
Enhancer Sequence | GTCTCTTTCT TTCTGTGTAT ATTAAGAAAA GAACATACTT TTCTACTTCA CTCTATTAAT 60
ATGATATATT ATAATATATG AAATCATTTT TATTCATTCT GAATTTGCTT TGTTTTCCTT 120
GGTCTCAAGG TACTAAAAAA AGAGCCCAAG GCCAGTACTC GGTGCTTGGA CCCTGGGAGG 180
TGAAGTTTAT CTGCTCTGGC AGCATGAAAG GCCAAAAGGG AAGCATTTTA CTGATTTTTT 240
TTATGGTTAG GACTAATTGG TAATCTTCCA AGATAGATCA ACCTGGATAA AATGATGATT 300
TCCTAGAAGG CAAGAAATCC TTGCTTGATA GTATTTTTTG TATGAGAATT CACTGCTCAC 360
CACAGGAACT TTCGTGAACA AGAAAAATAT TTACTTAGAT GAGACCCAGG AGATTATTCA 420
GTTAAAACAA AAAAGGTCAA GGTCTAAGGT CTTTTTTCTG GCCAACAGGG CACCATGAAA 480
TGCCCAGAGA CCTGTCTGTA GGATATGCAG TTGAACAAGT TGCAAAGATT CCAATGAATG 540
AGTCAGAGAA CAGAATCCTT CACTGCCGAG AGTGGTCCAT AAAAGAGTTG TGCCTACTTT 600
GATCTGGGAA TATTCGCTCT CTAATCTGAG AGTTCTATGG AAGCCTTGAC TTTGAGGTCA 660
GCGTCATTTG TTTTTATGTT TAGGGTGAGG CAAGGCCTGA CAAGGCTCCC TGGAGAATAG 720
GGTGTGGCCA GATCAGAGGC ACGTTGACCA ATTCCCAGCC CTTCCTCCCG TAAGAATCAG 780
CATGAGGGAG AGAGCCCAGG AGTGAGGAGG GGGGTCTCAG ATTGCTGGCC TTCAAGTTAC 840
AATGCCACCG CATCAGCAAC GGTGCATCAG CAAGGGAAGC AAGAGCAGAG GGGGAACAGA 900
GCCAGATGAT GGGGGAAGAG AGAACATGGG GATGAAGAGC AGGGAGCAGC CATAGAAGCT 960
GAAATTAGGC CACTGTGGAG GTGGCACGTC TGAGAACACA CCTGCTTGGG CCGCGGGGCG 1020
GGGGCTATGA GAGACACATT CTGGGGCTTA GCTCTGCCTT TTTTTTTGGT GCTACCCAAG 1080
CAAAGTAGCA TATGGAAGAG ATTTGATTTC TCCCCAAATG 1120
|
