| Tag | Content |
|---|
EnhancerAtlas ID | HS048-25481 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:47009730-47010960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr3:47010886-47010897 | TTTGTTTACTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_11155 | chr3:47006228-47021706 | CD20 | | SE_23114 | chr3:47010123-47010831 | Colon_Crypt_1 | | SE_40617 | chr3:47009514-47013782 | Left_Ventricle | | SE_41619 | chr3:47010076-47010853 | LNCaP | | SE_42118 | chr3:47006473-47013770 | Lung | | SE_58746 | chr3:46966845-47032612 | Ly1 | | SE_59747 | chr3:46966600-47033537 | Ly4 | | SE_60850 | chr3:46965041-47030117 | DHL6 | | SE_62445 | chr3:46966331-47033109 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH03I046968 | chr3 | 47010077 | 47010853 | | GH03I046970 | chr3 | 47010921 | 47011329 |
|
Enhancer Sequence | ATCCATTTTC TTCTTAATCT AACACTTTGC ACTAACACTC CATCTTCAAA AAATTAGGGC 60
TAGGATGAGT AAAGCCAGGG TGCAGGAGAA GGACCTCTTT GCTTCCACTG GAACCGGGCC 120
AGTTCCACCC ACTGTCACCC AGCGGAGAAG GCTGCAGGAC CACCTGGATG TCCCCACTTA 180
CAAGAGGGTA AAGAAGAAAG GACAGGCATC CACGTTTATA AAAGGCCTGT GTGCAAGATC 240
TCGAGCTAGA CACTTCATAG ACAGCATCTT TCTCTGTTCT CCTAGCTACT GATGAGTTCA 300
GAAGCTGTAT CTCGATTTTA TAGACAAGAG AGAGGCTCAG ATTTTTCAAG GCTTGCTCTG 360
AGTACCATAG ATGCGATTAA TGGAGCAGAG GTTTAAATCA GATCTGTCTC CAAAGTCCAT 420
TCTCTCCACT CCACCACTAG GCCTCCACCT GGCAGCCTGG TTACAGTTTA TATGTGTGAT 480
GGGTGGAGGC TCCTTCCCGG GAGGTACTTA TTCCCAAGCA CCTGGGGGTG AGAGGTGTAG 540
AGGGATAGAA GGCCAGAGCC TAAGGGACAA TCTAGGGTCA GCAACAACTC AAAGCACGAC 600
TGTGGGATGT TCCTTCAGCC CAGGGTTTCC TGGTCTATCA GACAGGGATG AAGCAATACA 660
CCCTGCTTCA AAGTCCTGCT TCAGGGATGG AACACGATTC TGCCACAACT GCCACGCAAA 720
TGTTATGACT GCCAACCTGC CAAAAGCTGT CAATACAGGC GGCAGTGATC GCCTTGGCTG 780
ACTTTGCAAC CAGGCTGCTG GGCCTGGGGA TGTGGCCACA TGGGATGTAG ATAGAGGCAA 840
CTTCTTGAGA CATGATCAGG ACACGGACAA GTCTGACTCC TCACCCAGCA TACTAGGCCT 900
CTCACCCACT GCCTCTGTTC CTCCAGCAAG ACTTGCTAGC CCCTCCCTCT GGTTCCCTCT 960
TTTACCCTCC CCCAACCTGG CCAGGGACCC TCCCTAGTAC TCCCAAGTCA GAGAGTACTA 1020
GTGCATGCCT TCTACCTTGG CATTGCTCCC ACTCTCTGCA CTGTGCATTT TTTTCTTTCT 1080
GTTTGTTTTT TAATCCTCCC ACCTCAGCCT CCCGAATAGC TGGGACTGCA GGAGCGGGCC 1140
ACCATGCCCG GCTAATTTTG TTTACTTATA TTTGTAGAGA TGGTGTCTTG TTATGTTGCC 1200
CATGCTGGTC TTGAACTCCT GAGCTCAAGC 1230
|
