| Tag | Content |
|---|
EnhancerAtlas ID | HS047-32015 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:151493150-151494300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr7:151494036-151494047 | GTTTTATTGGC | - | 6.14 | | PRDM1 | MA0508.2 | chr7:151494219-151494229 | GTGAAAGTGA | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09685 | chr7:151488264-151497337 | CD14 | | SE_27759 | chr7:151493037-151495146 | Fetal_Intestine | | SE_28667 | chr7:151492981-151495201 | Fetal_Intestine_Large | | SE_31948 | chr7:151493093-151494988 | Gastric | | SE_52790 | chr7:151493120-151495182 | Small_Intestine | | SE_65519 | chr7:151493090-151494738 | Pancreatic_islets |
|
| | 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 |
| GH07I151795 | chr7 | 151492888 | 151496138 |
|
Enhancer Sequence | CTATATGCTT GGATCTCTAG TCTTGGTTCT CCTTCTCTGC AGACCCCTCC TAACACAGAG 60
CCCTAGGCCC CCTCACCCGA GCTGGTGGGG ACAGACATGG GGAGAGTCCA GGGTAAAAGC 120
AGGCCGCTGT TTGGAAGCTC TCAGCCTTCG CTGCATAGAC GGATGGGTCT GCTCAGTCAT 180
CGGGTGGGCT CTCCGCCCAC ACTGTGGCTC TCTGTCCACA CTATGGAACC CTCACTTTGC 240
CCAGGGCCCA GTGAGACACC CACAGGCCCC AGCTGGACGA GAGGACAAAG ACGGATGTGA 300
AGGGCCGTTG TCCTGGCAGT GCTTAGAGAA CAACAGGAAA TGGCCAAATG TCCTCCTTTG 360
ACTGTCAGGG AACATTCACA GTACGTGAAG GGCAATCACA GGTTTAGAAA AGCACCACGA 420
TCACCTCCTA GCCTCGTCTC TGAGCCTTGG CAGCAGAGTG GGGCAATCCT CTTGCCTTCG 480
CACGCTGGGT AACAGTCGTG CAAGTGTCTG TCATGGCATC TTGTCACCCT GTCCTGTCAC 540
TGAGGGCCTG TCTCCTGCCA CACCCAGTTG GAGCTCGGCA AGGACCGCGT CTTTTTCACC 600
CCTGAGTCAC CGGCTCCTCC CAGGGCTGGA TTCCATGAGC CTCTGTCCTT CCCCTTCGCA 660
GAGCTGACAC GGGGAGAGTG GTCATAAGCT GGGGCGTAAA TGACTGAGGA CGGCCCGGGG 720
GCCAGTAAAC ACCAAGACCT CGGGATAAGG GAATGACATC CTGATGCGCC ACCTCCAGCC 780
CCTGTACGGA GGGAACAGCC CTTCATTTCT AGGACTGTCT TCAGCTCTGA CATTATGATT 840
CTACCAAGAC AGGGTGTGAA AAGGCCAGCT CTGGGGTTCT GGGGAGGTTT TATTGGCTCG 900
CAAATAAAAT GCCAAACCAC CAGCCAATAC CAGCATAGAG CCCTCCGTGG GCACTACCGA 960
CTCAAGGGAA AGGCCCCGAG GCCCCACACC CGGCCCGGCC AGCCAGCTGC AGACACACCC 1020
TCCAGTCATC GGCCACCCAG ACTTCAGAGA GGAAAAAACC AGCCACGAGG TGAAAGTGAG 1080
ATGGCCCCGG CCTGACCTCT GCTGCAGAGG CCCAAATGGC CCTGGTCAGA TCTGACGCTT 1140
CCCCCACAGT 1150
|
