| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06374 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:121396580-121398250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr12:121398131-121398145 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23495 | chr12:121396589-121398166 | Colon_Crypt_1 | | SE_24673 | chr12:121396725-121397868 | Colon_Crypt_2 | | SE_24673 | chr12:121397874-121398148 | Colon_Crypt_2 | | SE_27808 | chr12:121395970-121401773 | Fetal_Intestine | | SE_28751 | chr12:121395949-121401811 | Fetal_Intestine_Large | | SE_53251 | chr12:121396633-121398199 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 121397539 | 121398109 | | chr12 | 121396901 | 121398191 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I120958 | chr12 | 121396119 | 121401634 |
|
Enhancer Sequence | CTCCCGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCAAG TAGCTGGGAT TACAGGCATG 60
TGCCATCATG CCCAGCTACT TTTTTTGTAT TTTTAGCAGA GACAGGGTTT CTCCATGTTG 120
ATCAGGCTGT TCTTGAACTC CCGATCTCAG GTGATCCACC TGTCTCGGCC TCCCAAAGTG 180
CTGGGCTTAC AGGTGTGAGC CACCGGGCCC GCTGTTTTCA TTAATTTTCA TTTGAAGACA 240
TCCTGATACC TAGTCAAAGC CTCATGACTT TGGGGGCTGA GAGGACAGGG TGGTGGTGGA 300
TGTATAGTTG GCGGGGTGTG GTGGTGCACA CCTGTAGTCC CAGCTACAGG AGGATTGCTT 360
GAGCCCAGGA GGTCGAGGCT GCAGCAAGCC ATGAGTGTGT CACTGTACTC CAGCCTGGGC 420
GACAGAATGA AACCCTGTCT CTTAAAAAAA AAAAAAGAAA AAAAAAGGAT GTACAGTAGG 480
AGGATTATCT TTGCCTTCAG TTGCTGGGAG GTGATCTCTA GGCCCCTTAA CGTCCTGTCT 540
GATGGAAGTG TCTGTGTTTG CCTGGGGCCT TTGGCCACCA GATAGTCTAA CAATGTGATC 600
TGTAATGAAG GCTTTGGAAC ATCCTGTATC AGTTCCAACC TCCAGATGAG CTGGATACAC 660
AAGAGTTAGC TCAGGAGAGA CTGGAGATGA AAGGTCAGCC ACACTGGCAG TAAGGGATCA 720
AGCCCCACTA AAAAACGCTG GACACTGGCT GGCAGTGGCT CATGCCTGTA ATCCCAGCAC 780
TTCAGGAGGC TGAGGGGGGC GGGTCACCAG ATGTCAGGAG TTTGAGATCA GCCTGGCCAA 840
CATGGTGAAA CCCTGTCTCT ACTAAAAATA CAAAATCAGC TGGGCATGGT GCATGCCTGT 900
AATCCCAGCT ACTCGTACTC TGGAGGCTGA GGCGGGAGAA TCGCTTGAAC CCAGGAGGTG 960
GAGGTTGCAG TGAACTGAGA TCACGCAACA GCACTCCAGC CTGGGCGACG AGAGCGAGAC 1020
TCCATCTCAG AAACAACAAC AACAAAAACA AAACCCCCAA AAACGCTGGA CACCAAAGCC 1080
TCAGGAGCTT CTCTGGTTAG CAGTATTCTC TGAGTGTCAT CACGCATCAT AGCTGGGGGG 1140
AGGTGACTGT CTGGAGAGAA GGTAACTAGG AGCTTTGCAC TTGAACCCCT TCCGCACCTC 1200
ACCCTCTATG TCCTTTCTTG TGGCTGGTTC TGATCTGTGT CTGTTTGCTA TCATAAAAAC 1260
TGTCGTTATG AGGCGGGGCA CTTTCCTGAG TTCCATGAGT CATTCTAGTG AATTATTGAA 1320
CCACAGGGGG TAGTGGGAAC CCTCAATGCA GCCAAGCGGT CAGAAGTGAG GGTGGCCCAG 1380
GAATCCCCAG TTGCACCTGG CATTTGAAGT GAAGGCTGCC TTGTGGAGGG ACTGTGTCCT 1440
TAGCCTTGAG CTTGACAAAT TCATTGCAGT AGGTTCTGTC ATCTGCCTCT TAGAGAATAC 1500
CCTCATTTCA ACTGGGCGCG GTGGCTCACG CCTGTAATCC CAGCACTTTG GGAGGCCGAG 1560
GCGGGCGGAT CACGAGGTCA GGAGATCGAG ACCATCCTGG CTAACACGGT GAAACCCCGT 1620
CTCTACTAAA AATGCAAAAA ATTAGCTGGG CGTGGTGGCG GGCGCCTGTA 1670
|
