| Tag | Content |
|---|
EnhancerAtlas ID | HS146-03028 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr11:100746790-100748570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr11:100746918-100746929 | TTTGACCTTGA | - | 6.14 | | Esrra | MA0592.2 | chr11:100746919-100746930 | TTGACCTTGAA | - | 6.14 | | RUNX1 | MA0002.2 | chr11:100746885-100746896 | AAACCACAGAA | - | 6.32 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I100875 | chr11 | 100745975 | 100749537 |
|
Enhancer Sequence | CTGAAACAAA TTTCAGTCCT TACCTTTGCA AAATACCTTC TCTGGTAGCA CAAACTTAAT 60
AACATGTGTT TGATAATTTG GCTTCCTATG TTGGAAAACC ACAGAATTTA CAGCAAGATG 120
AACTTGAATT TGACCTTGAA CAAATTTGTG GCTGAAAATA ATATTCTTAA CACAGACACC 180
ACAAATTTTT ATTTCAAGTA TTTTTATTTT CATGGAAACC TTTTACCTTT GAAGAAAATA 240
TATACGTTCT TAGTTTAGGG CTATAGCTTA GCACACAAGC AATATAGAAG AGAAAAATAA 300
AGAATCCTTT TTGCTTCTGT AGTTGGACGT ATTTAAATAT TTAAGAGAAG GTCAGGTAAA 360
AACACTTTAC AATCAGATGC TTTTATTTAG TTTTCAGAAC TGCTAAATAT GGTGGACAAC 420
CATCCTCCCA ACAACATTTG TTATTTTAAG TAAGAATGTG GTGAATCTCA TCACGGATTT 480
GTCTGTATGC ACTGCTTTTA CTTTATACAA AATCAGCCAA TTAAAAAGAA AAAATTATTT 540
TGTTTCCTTG GGATTGTGCA GATAAGTGAA CTCATTTGTT AGCCAACATT ATTGAAATCT 600
GTGGGTATGT TTGTGTAGAC TCAGCCCTAG AGCAAGCAAT ATATTTGCAA CTGAACACAT 660
ATATTGAGAG AAATCTGGTA AGCTCTACCA TTTATATTCA TCATAGTAAA CAGCTCACTG 720
ACTTTATTAA TAGGTTTCAC TTAATACAGC TTCTTACTGT TCTGTATTTA GAGTTGATTT 780
TACGTCTTTC TCTTCTATAT ACAGCCAGTA ATAATCTGAA GCCAAATTTA ATGCTCTCCA 840
GAGACCATGC AACCCACGTT TGCATCAAGA GCCTGGTGAT TTACAGACTC TGAGTTGGAG 900
AGATGACCTC TACAATTACT GTAGAAACCC AGTGAGAAGT GAAGTGAGCT CACTGTAGAA 960
AGATTTCAGG CATTGAAAAA ACTTGCCTTA TTTGGTAAAT GTGGTTAACT GGTCCCAGCT 1020
GGTAATACTG GTGAGCTCAT TGTGAGATGT ATTGTCTCTT AAAGCCAAAT TCTTGTATTT 1080
TTAAAAATCT GTTAGAATTG GAGTATTAAA TAGTATTTGT TCAGTTTTTC TTGATGTTCT 1140
AGGAAGTAAA TCAAATCAGA AACAATAGAG TTCCATTTTG AAAACTAAAG CTCAGATGCA 1200
GTGACACTTA AAATATTCCC AGTATATCTT TTCTTGTCTC TTATGTTGCT TACCTTACTT 1260
AGCCTCTGGG GAATTTGGAG TTTAATTTAT GCCTTGAAAT ACAAGACTCC TACGGGAAGC 1320
AAATTTATGT GGCCATGTGT GCTTTACTAT ACTTCTTTGC TCATGTAAGT TTACTCTGTA 1380
TATTACACTT TCAGGATAGA TTCTGTTAAT TGCATTTTCT TTAATGACCA GTAGCATTTC 1440
ATGCTTGTAA ATGAAAGACT ATGGTTTCTC ATGTCTTCTG TAAAATTCCT ACCTCAGATT 1500
TGTCTGTATC TTGAGTCTGG CTTTCCAGAG ATTCAGTTGT TTCAGAGGAA AAAACACAGG 1560
GTTTAAGTCA AGGAGAACTT GGTTTGAATC CTGGCTCTGC TGTGTGTGAA CTTGATGACT 1620
TCAGGACAGC TCCTTAACTG TTGTGACAGT TAAGAGGTGT TACCAGGGTG GGCGCGGTGG 1680
CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGCAG GCAGATCACG AGGTCAGGAG 1740
TTCGAGACCA ATCTGGCCAA TGCAGTGAAA CCCCGTCTCC 1780
|
