| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00760 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:27487810-27488970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:27487853-27487868 | CGAACTCTTGACCTC | - | 6.24 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_09350 | chr1:27487738-27488871 | CD14 | | SE_23485 | chr1:27487857-27489118 | Colon_Crypt_1 | | SE_24258 | chr1:27487876-27488266 | Colon_Crypt_2 | | SE_24258 | chr1:27488306-27489028 | Colon_Crypt_2 | | SE_31553 | chr1:27487818-27489086 | Gastric | | SE_50517 | chr1:27487684-27489162 | Sigmoid_Colon | | SE_52500 | chr1:27487781-27489130 | Small_Intestine | | SE_53642 | chr1:27487793-27489132 | Spleen |
|
| | 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 |
| GH01I027161 | chr1 | 27487772 | 27489011 |
|
Enhancer Sequence | TTTTTGTAGA CACAGGGTTT CACCATGTTG GCCAGGCTGG TCTCGAACTC TTGACCTCAG 60
GTGATCCACC TGCTTCGGCC TCTAAAAGTG CTGGGATTAC AGGCGTGAGC TACCACACCC 120
GGCCAAGTCC TCATTTTTTA ACCATTCCAG GCCCACACTG CTTTTGACTC GGAGAGGCCA 180
GGTCTCTGCA GACCCTTCCC CTGCAGATCC AGGACAGCCT CAGGAAGCCT GGACCCTGGG 240
TGGCATCTCC CCCTGCTTAA GCCATGTCTG CTCCCCAATC CCCTCCTTGA ATCCTTTCAC 300
TAAAAGTGCC TGGAGTTTTA TGGCACAAAA TGCATGGCCC TAGGAAAGAA TCTGCTCAGC 360
CCCTATTAGC TGCGCATTAT GAGCAAGTCA CACCTTGTTT CTGTCTCTCG CTGTGTTCAT 420
GTATATGAAA GCTGGGTGGA GTCACATTAC TTGCTTTGTA AGGTTTATTG TAAGGATGAA 480
AAGGCCACTG TATGTCAAGC ATAGTTCCTG GTACACAGTC AGCACGCAGT GACTGGGTTC 540
ATTTCCTTCT TTTGTTTTTT TTTTTTTTTG AGACAGAGTC TTGCTGTCAC CTAGGCTAGA 600
GTACAATGGT GCAATCATAG CTCACAGCAA CCTCAAACTC CTGGGCTCAA CCGATCCTCC 660
AGCCTCGCCC TCCCGAGCAG CTTGGACTAC AGGTACATGC CACCACACCT GACTAATTTT 720
TAAAAATATT TTTGGTAGGG ATAGGGTCTT ACTATATTGC CCAGGCTGGT CTCAAACCCC 780
TGGTCTTGAT TGATTCTCTT GCCTGGGCCT CCCAAAGTAT TGGGATTACA GGGGTAAGCC 840
ATTGTACTCA GCCGCTCCTT CTTTCATCAT AATGTCACAG CCCAGCAAAG CCTTCTTCCA 900
GTCTCCCCGG CACTCACTTC ACCACTGCCT CCTTCTATTT CTCAAACACT GGCAGACACA 960
CTTCTGCCTC AGGGTCTTTG CACTTGCTAT TCCTTCTGCC TGGAACACTC TTCCCCAGAT 1020
ATCCACATGG CTGGTTACCT GACCTCCTTC AAGCCTTTCT GCGAATCTCG CTTCCTGACA 1080
TGGCCTACTA TGTTATAATC CTATGTAATA GTGACACTTC CCCTGCCTGG CCACCACCAC 1140
TACCACCCAG CCCCTTCCCC 1160
|
