| Tag | Content |
|---|
EnhancerAtlas ID | HS182-20428 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:151493200-151494890 |
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 | | RREB1 | MA0073.1 | chr7:151494312-151494332 | ACCCCCCCCACCCCCCACCG | + | 7.1 | | ZNF740 | MA0753.2 | chr7:151494310-151494323 | CCACCCCCCCCAC | + | 7.52 |
|
| | 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 | TAACACAGAG CCCTAGGCCC CCTCACCCGA GCTGGTGGGG ACAGACATGG GGAGAGTCCA 60
GGGTAAAAGC AGGCCGCTGT TTGGAAGCTC TCAGCCTTCG CTGCATAGAC GGATGGGTCT 120
GCTCAGTCAT CGGGTGGGCT CTCCGCCCAC ACTGTGGCTC TCTGTCCACA CTATGGAACC 180
CTCACTTTGC CCAGGGCCCA GTGAGACACC CACAGGCCCC AGCTGGACGA GAGGACAAAG 240
ACGGATGTGA AGGGCCGTTG TCCTGGCAGT GCTTAGAGAA CAACAGGAAA TGGCCAAATG 300
TCCTCCTTTG ACTGTCAGGG AACATTCACA GTACGTGAAG GGCAATCACA GGTTTAGAAA 360
AGCACCACGA TCACCTCCTA GCCTCGTCTC TGAGCCTTGG CAGCAGAGTG GGGCAATCCT 420
CTTGCCTTCG CACGCTGGGT AACAGTCGTG CAAGTGTCTG TCATGGCATC TTGTCACCCT 480
GTCCTGTCAC TGAGGGCCTG TCTCCTGCCA CACCCAGTTG GAGCTCGGCA AGGACCGCGT 540
CTTTTTCACC CCTGAGTCAC CGGCTCCTCC CAGGGCTGGA TTCCATGAGC CTCTGTCCTT 600
CCCCTTCGCA GAGCTGACAC GGGGAGAGTG GTCATAAGCT GGGGCGTAAA TGACTGAGGA 660
CGGCCCGGGG GCCAGTAAAC ACCAAGACCT CGGGATAAGG GAATGACATC CTGATGCGCC 720
ACCTCCAGCC CCTGTACGGA GGGAACAGCC CTTCATTTCT AGGACTGTCT TCAGCTCTGA 780
CATTATGATT CTACCAAGAC AGGGTGTGAA AAGGCCAGCT CTGGGGTTCT GGGGAGGTTT 840
TATTGGCTCG CAAATAAAAT GCCAAACCAC CAGCCAATAC CAGCATAGAG CCCTCCGTGG 900
GCACTACCGA CTCAAGGGAA AGGCCCCGAG GCCCCACACC CGGCCCGGCC AGCCAGCTGC 960
AGACACACCC TCCAGTCATC GGCCACCCAG ACTTCAGAGA GGAAAAAACC AGCCACGAGG 1020
TGAAAGTGAG ATGGCCCCGG CCTGACCTCT GCTGCAGAGG CCCAAATGGC CCTGGTCAGA 1080
TCTGACGCTT CCCCCACAGT CAGCTTCTTG CCACCCCCCC CACCCCCCAC CGCCGCCTGG 1140
TGCTCCCCAC CGGGTACACA CCCAGCGGTT TTGGTTAGTG CTTGAAGACA AACTGCAGGA 1200
GGGACACCAT GAACTACAAT AAAATTGGGC ACCCTGGGGA CATTTTTGTA AGGTCACCGA 1260
GTTGCTGGCT GGCTCTGAGA CACACCCTCC TCTACGTAGA GGACCTTGTG TGAGAGAGGA 1320
CACCTCTGAA CGAGGGCTCA GAGACCTCAT TTCTGCTCCC AAACAGCTAC CCAAGATGTG 1380
GCTTTGGGCT TTGGCCCAGA GCTGAGGCCT GCAAAGGCTG CCACCTCAGT GCTTCCAGAA 1440
TCTCAACTGT CCATATTTAC AGAGCCATAC ATCAAAAGAT TCTTCCCCAA CACTTTCTAC 1500
GGGTACCCAA GGACTCCTTC TACTCCATCT TGTTTCACCC ACCTGCTCTG TGCCAGGCAC 1560
ATTATAGATC AAAAGGTACA GGGAGTTCAG AGGAAGGAGG AAATACCATG GACTTAAAAA 1620
GCAAGCCAGG GCTTCCCAAG CCAAGCATAG TGAATAGAGG AGCTTTCATT TGTCTCCTCA 1680
CTTCCATCCC 1690
|
