| Tag | Content |
|---|
EnhancerAtlas ID | HS052-19886 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr2:26239950-26241800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TEAD1 | MA0090.2 | chr2:26241773-26241783 | CACATTCCAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_09566 | chr2:26240304-26241810 | CD14 | | SE_26712 | chr2:26239870-26242089 | Esophagus | | SE_28420 | chr2:26240306-26241937 | Fetal_Intestine | | SE_29154 | chr2:26239992-26242119 | Fetal_Intestine_Large | | SE_32014 | chr2:26240172-26241573 | Gastric | | SE_35193 | chr2:26240079-26241982 | HeLa | | SE_36382 | chr2:26240216-26241937 | HMEC | | SE_64640 | chr2:26240168-26241940 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 26240135 | 26241696 | | chr2 | 26241064 | 26241266 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I026016 | chr2 | 26238975 | 26240088 | | GH02I026017 | chr2 | 26240097 | 26242426 |
|
Enhancer Sequence | CCTCCCAAAG TGCTGGGATT ACAGGCAGGA GCCACTGCAC CCAGCCTTTT TTTAAAACAA 60
GGTCTTACTC TGTCGCCTGG GCTGGAATGC AGTGGTATGA TCTCAGCTCA CTGCAACCTC 120
TGACTCCTGG GCTCAAGCAA TCCTCCCACC TCAGCCTCCT GAGTAGCTGA GACTACATGC 180
ATGCACCACT GCACCTGCCA TTTTTTCCGG ATTTATAGAG AGAGGGTTTC GCCATGTTAC 240
CCAAGCTGGT CTCAAACTCC TGGGCTCAAG CCATCCTCCG GCCTCAGCAT CCCAAAGTAC 300
TGGGATTATA GGCATGCACC ACTGCACCAG GCAAGGACAC AGATTTTTAT TGTTCACCCA 360
CAAAGTGCTT CACATGCACT ACTTTGTCTG ACCCTCACGA CAACCTGCAA GGTAGGTATT 420
GTATTCCTAC TGTACGGATG AGAAAAACTG AGACTCACAA AGGTTAGTTA CTAGCTCAAG 480
ATCATGTATG CCTCAGTGGC AGGGCCAGGA TTCAGAGCAG GGTGGCCTGG AGGTCTGAGG 540
TTGGAAGCAG GTGTCACCTT AATGACTTAG GAATGAGGTC AGTGTCTGTG TCCTCCAATT 600
ATGGTGCCAG GCTCAGTCTC TACGAATGCC TGGAGAATAT GTCAGCACTT ACTGTAGCTT 660
CATGTTTAGG CCAAGAAAAG GCTGAGATGA GATGATCCAT GAGAGTTTTT CACAGAAACA 720
CAGACCAAAC ACAGAAGCAA AATCTTGGTC TTCATATTGC CCCAGACTTG TTCTCTTCTG 780
GGACTGAACC TAGTGTTAGA ATCCTGCTCT GCAGGAATAG GGGGGTGTCT TTACATTTCA 840
TTCTGGTTAT TTGCCTAAAG CAAATCCCAG AGATACCCAG AGAGGGAAGA CTTTCCTCTG 900
CAGATGGTGG AAGATGCTGG CGCCCAGGCC ATCCTATGTC ATCTGTATCC AGACACAGAT 960
TCCAGATCCC TGTTCATGCC TCTGAGGACA TGGAGCGGGC CTTTTAGCTC TCTTCAGAGC 1020
TAGAGTTTCA GGCATATGGT TGCTGCCCTG GATGACAAGG GTAGCACATG GGTGGGAACT 1080
CCAGATGCAT GTAAGGGAGC AAGAAGCTGC CCACTGAGGA GAATGCTGGG ATAGTGCAGG 1140
GCTGGGCTGG CCCAACTAGT TCAGCTCAGC CAGGAAAGGG CAGGTCAGAT CTGGCTCAGC 1200
AGGGGAGGCT GTGTCGGGGA GTGGTGCTGA CTCAGGGCCT GGTGAGTCAG GTGACAGCCA 1260
AGGACAGCTG TTGCCTGGGT GTTTTTAGAA AACTTTGGCT GCCAACCACT CTCTCATGGG 1320
TGCTTCTGCA CCTACTCAGA AGCAGGCAGA AAAAAGGAGG GCATCTTCTG TATAAGAAGC 1380
TCTGGGTGAG GGGTATTAAT ATCTGGCTCT ACTTATGTTG ATCCTTCCCA TGAAGTACCT 1440
AGAAAACGGA GCAGAAATTA ATTGAGAGGC TTCCAAATCC CTTCTGAATT CTCTGAAAAT 1500
CACTTATCTT TTCTGCTTAG CTCTTTTTAG GCACCTTGCC AGGTATCCAG CATAGAGGTT 1560
AAGAGAGCAG GCTCTGAAGT TAGGAGGGCC TGGGATCAAA ACCTAATTTC ATCATTTATA 1620
GTTGTATGAC TTAGATCAGA CTAAAAACAA CTTTTAATTA TGGAAAGCTT CAAATATATA 1680
TGAATGACAC ACATTAGTAT GATGAACCTC CATATACTCA TTATCCAGCT TGAATAATCA 1740
TTAACCCACT GTAACTTTAT TTCATCTATA CTCTACTTAT CCCCTTTGCT CCCACTTATT 1800
TTGAAGGAAA TACCAGGCAT CATCACATTC CATCTCTTTT TTTCTTTTTT 1850
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