Tag | Content |
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EnhancerAtlas ID | HS108-21737 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:26240440-26241660 |
| 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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I026017 | chr2 | 26240097 | 26242426 |
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Enhancer Sequence | CCTCAGTGGC AGGGCCAGGA TTCAGAGCAG GGTGGCCTGG AGGTCTGAGG TTGGAAGCAG 60 GTGTCACCTT AATGACTTAG GAATGAGGTC AGTGTCTGTG TCCTCCAATT ATGGTGCCAG 120 GCTCAGTCTC TACGAATGCC TGGAGAATAT GTCAGCACTT ACTGTAGCTT CATGTTTAGG 180 CCAAGAAAAG GCTGAGATGA GATGATCCAT GAGAGTTTTT CACAGAAACA CAGACCAAAC 240 ACAGAAGCAA AATCTTGGTC TTCATATTGC CCCAGACTTG TTCTCTTCTG GGACTGAACC 300 TAGTGTTAGA ATCCTGCTCT GCAGGAATAG GGGGGTGTCT TTACATTTCA TTCTGGTTAT 360 TTGCCTAAAG CAAATCCCAG AGATACCCAG AGAGGGAAGA CTTTCCTCTG CAGATGGTGG 420 AAGATGCTGG CGCCCAGGCC ATCCTATGTC ATCTGTATCC AGACACAGAT TCCAGATCCC 480 TGTTCATGCC TCTGAGGACA TGGAGCGGGC CTTTTAGCTC TCTTCAGAGC TAGAGTTTCA 540 GGCATATGGT TGCTGCCCTG GATGACAAGG GTAGCACATG GGTGGGAACT CCAGATGCAT 600 GTAAGGGAGC AAGAAGCTGC CCACTGAGGA GAATGCTGGG ATAGTGCAGG GCTGGGCTGG 660 CCCAACTAGT TCAGCTCAGC CAGGAAAGGG CAGGTCAGAT CTGGCTCAGC AGGGGAGGCT 720 GTGTCGGGGA GTGGTGCTGA CTCAGGGCCT GGTGAGTCAG GTGACAGCCA AGGACAGCTG 780 TTGCCTGGGT GTTTTTAGAA AACTTTGGCT GCCAACCACT CTCTCATGGG TGCTTCTGCA 840 CCTACTCAGA AGCAGGCAGA AAAAAGGAGG GCATCTTCTG TATAAGAAGC TCTGGGTGAG 900 GGGTATTAAT ATCTGGCTCT ACTTATGTTG ATCCTTCCCA TGAAGTACCT AGAAAACGGA 960 GCAGAAATTA ATTGAGAGGC TTCCAAATCC CTTCTGAATT CTCTGAAAAT CACTTATCTT 1020 TTCTGCTTAG CTCTTTTTAG GCACCTTGCC AGGTATCCAG CATAGAGGTT AAGAGAGCAG 1080 GCTCTGAAGT TAGGAGGGCC TGGGATCAAA ACCTAATTTC ATCATTTATA GTTGTATGAC 1140 TTAGATCAGA CTAAAAACAA CTTTTAATTA TGGAAAGCTT CAAATATATA TGAATGACAC 1200 ACATTAGTAT GATGAACCTC 1220
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