| Tag | Content |
|---|
EnhancerAtlas ID | HS048-38985 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chrX:122918010-122919470 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chrX:122919031-122919043 | GCAATCACTGCA | + | 6.14 | | NFAT5 | MA0606.1 | chrX:122919331-122919341 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chrX:122919331-122919341 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chrX:122919331-122919341 | AATGGAAAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29234 | chrX:122918370-122919643 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI123784 | chrX | 122918024 | 122919388 |
|
Enhancer Sequence | AAAATTAGCC GGGCATGGTG GCAGTACCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAG 60
GAGAATTGCT TGAACCCAGG AGGCAGAGGT TGCAGTAAGC TGAGATTGCC CCATTGCACT 120
CCAGCCTGGG CAACAGAGTG AGACTCCTAC TCAAAAAAAA AAAAAAAAAA AAGTTGGCGG 180
ATGCGGGGAC AGCAAAGGGC TTAAGTAGAC ATTTCTTCAA AGAAGATATA CAAATGGCTG 240
ATAAAGACAT TTAAAGATAT TCAGGGCCAG ACGTGGTGGC CCACATCTAT AATCCCAGCA 300
CTTTGGGCTG CCAACGTGGG AGGATATCTT GAGCCCAGGA GTTCACGACC AGCCTGGGCA 360
ACATAGTGAG ACTATCTCTA CATAAAAACA AAAAATAAGG CTGGGCATGG TTGCTCACAC 420
CTGTAATCCC AGCAATTTGG GAGGCCGAGG CAGGCAGATC ACCTGAGGTC AGGAGTTTGA 480
GACCAGCCTG GCCAACGTGG CAAAACGCTG TCTCTACTAA AAACTACAAA AATTAGCCTG 540
GCATGGTGGC GGGCGCCTGT AATCCCAGCT ACTTGGGAGG CTGAGACAGG AGAATCGCTT 600
GAACTTGGGA GGCCGAGGTT GCAGTGAGCC GAGATTGAGC CATTGCACTC CAGCCTGGGT 660
GACAGAGCAA AACTCCATCT CAAAAATAAA TGACTAAATA AAATAAAGAT GTTCAACATC 720
ACTAATCACT AAGGAAATGC AAACCAAAAC CACGAGATAC CATTTTACAT GCAGAAGAAT 780
GGCTATAATT TTAGAAAGAT AGAGTTTCAC AAGTCTAGAC GCTGAGCCGC AGCACATTTG 840
CAACGTCACG TGGAAGCTGA AACTGCACCT CCCACGTGGC CCCTCTAGCC AGCTGAGAAC 900
CTCAGATAAG AACTACACCC AGGCCAGCAC CAGCAGCTCA GCCACTAGCA GCAGCCCCAC 960
CCTCTGCAGC TGGCTCTCCT GCTGCTGCAC TCCGCGGCAG CCAGGTCTGA TGGCCCGGGC 1020
GGCAATCACT GCAGCTGGCA TGGCTGTGGA CTCTGCTGTG GGGCACATAC TGGGTCATGC 1080
CATCAGTGGG AGCTTCAGTG GAGTAAATAA TGCTGAGCCC CCAAGTGGTG ACATCACTTA 1140
CCAGAAGCCT CAGGGAACCC ACCCGGCACA GCAGCAGTAG GCTTTCTTGT ATGAGATAAA 1200
ATGGTTTTTG GAATGTGCCC AGAATCAGGG AGACATAAAG TTCTGTGAGG GTTTCCATGA 1260
GGTGGTGAAA CAGTGCAGAC TTGCAAATGG ATTTATCTAA TCAAGAAGTT CAAATTGAAG 1320
AAATGGAAAA TCAGCTCTCA CAACTAAGTT AATTTAGCAT AAAAACATAA TTGATAGCCG 1380
GGCGTGGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCCGAGGCAG GCGGATCACC 1440
TGAGGTGGGG AGTGCGAGAC 1460
|
