| Tag | Content |
|---|
EnhancerAtlas ID | HS048-01750 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:85967470-85968730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:85967629-85967650 | TCTTTCACTACCTTCTCCTCC | - | 6.09 | | ZNF263 | MA0528.1 | chr1:85967641-85967662 | TTCTCCTCCTCTTTATCCTTT | - | 6.21 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_45583 | chr1:85965516-85968920 | Osteoblasts |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 85968002 | 85968172 | | chr1 | 85968200 | 85968639 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I085501 | chr1 | 85967481 | 85969230 |
|
Enhancer Sequence | TTACAGCTAT TTATGGCAAG AGGGCTGGTA CTAGTAACTT CATCAAAGCC AGAAGCAGAA 60
GTCCTTCACA CTGGATACTT TTGCTCATCA TCTCCTGTTT GAAATTCTCC CTGGTTTTTA 120
GAACTCTAAT CTTGATTTTC CTCCTAAATT TCTTATTATT CTTTCACTAC CTTCTCCTCC 180
TCTTTATCCT TTAACCATGC TTCCCATGCC TAAATTATAT TCATTCTTTA AAATCCAAAC 240
TTTCTCCATA AAGCTTATCC AGTCTGCTAC GCTGGAATTT ATGCCAGGTA TAAGTATATA 300
TGAACATACT TAACACTTTA TTGGCACTGC TTCAGACAGC ACTTTGCACT TTCTGCCTTT 360
TGAACGATCA TGTCACTTCC ATATTGTAAA CTCTTTGAAG ACACGGACAA TGTCTAATTT 420
ATCATTGTTT CTTCCTCAGA GCTTAACACA GTATTCCTCT ATTCACCTTT AATTCTGATA 480
TGGTGCTACT GGTGGTTGCC CAACAACGAG AGGAAACGAC ATTTGCTGAC TACACCCCAC 540
GCACTCTGCT AGATGCTTTG CACATGTTAT CTTGCTTAAT TCTTGAGAAT GATACTGAAA 600
AGTAAACACA ACCAAATGAC AACAAAGCCA GTGGCTCTGA CTGAGATCAC ACATGCTCAA 660
CTGCTGGAAT TTCAGTTCTT TGAATCTCTT CCTTTCTCCT GGGAAAATGT GACACTTTTG 720
AGGACCTCCT TGCTGTCCCT TGCTTGTCAC TGCCATCATT GCCCCCTTCT CAGATCCCTC 780
TGGCTTCAGC CTGGTAAGAG GCTGCTTCCC ATCTTAGTAC CTCCCTAAGA AGTTTTTCTT 840
GTGGCATCAC CACCACTGCT GCTTCCACCT ATCCCCACCG CCACCACCAC TGCCATTGTT 900
TCTGCAGTGC TGCAGCCACT GGTACAGGGC TGCTCCAGGC CAGGCAGTTT CTCACTGAAG 960
CCTGGCCTGC ATTAAAGAGT CCTCTTTTGC TGCTTCTCTT CTGGGTTCTC CAGAGATAGC 1020
CCTGCCTCTC CTGCCTCCTA CCACCTCTGT CTGCAGAGCC ATGGGGAAGC CCTGGAGGAG 1080
TCACACTACC AGAACACTCG GGGCCTCTGC CTGCCTTTGT CTCCTGGAGT CAGATCTGCT 1140
TCTCCTTCAG CCAGATTTTC TCACTATCCA TAGCTACCAG TCAGTGGATT GATGTCCCCC 1200
TGGTGGTGGA TCTCATTGAA CACGGACTCA GTAAATTGTT AAGTGTTTGC TAAGAACTTT 1260
|
