| Tag | Content |
|---|
EnhancerAtlas ID | HS193-17301 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr2:26240190-26241600 |
| | 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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I026017 | chr2 | 26240097 | 26242426 |
|
Enhancer Sequence | CCAAGCTGGT CTCAAACTCC TGGGCTCAAG CCATCCTCCG GCCTCAGCAT CCCAAAGTAC 60
TGGGATTATA GGCATGCACC ACTGCACCAG GCAAGGACAC AGATTTTTAT TGTTCACCCA 120
CAAAGTGCTT CACATGCACT ACTTTGTCTG ACCCTCACGA CAACCTGCAA GGTAGGTATT 180
GTATTCCTAC TGTACGGATG AGAAAAACTG AGACTCACAA AGGTTAGTTA CTAGCTCAAG 240
ATCATGTATG CCTCAGTGGC AGGGCCAGGA TTCAGAGCAG GGTGGCCTGG AGGTCTGAGG 300
TTGGAAGCAG GTGTCACCTT AATGACTTAG GAATGAGGTC AGTGTCTGTG TCCTCCAATT 360
ATGGTGCCAG GCTCAGTCTC TACGAATGCC TGGAGAATAT GTCAGCACTT ACTGTAGCTT 420
CATGTTTAGG CCAAGAAAAG GCTGAGATGA GATGATCCAT GAGAGTTTTT CACAGAAACA 480
CAGACCAAAC ACAGAAGCAA AATCTTGGTC TTCATATTGC CCCAGACTTG TTCTCTTCTG 540
GGACTGAACC TAGTGTTAGA ATCCTGCTCT GCAGGAATAG GGGGGTGTCT TTACATTTCA 600
TTCTGGTTAT TTGCCTAAAG CAAATCCCAG AGATACCCAG AGAGGGAAGA CTTTCCTCTG 660
CAGATGGTGG AAGATGCTGG CGCCCAGGCC ATCCTATGTC ATCTGTATCC AGACACAGAT 720
TCCAGATCCC TGTTCATGCC TCTGAGGACA TGGAGCGGGC CTTTTAGCTC TCTTCAGAGC 780
TAGAGTTTCA GGCATATGGT TGCTGCCCTG GATGACAAGG GTAGCACATG GGTGGGAACT 840
CCAGATGCAT GTAAGGGAGC AAGAAGCTGC CCACTGAGGA GAATGCTGGG ATAGTGCAGG 900
GCTGGGCTGG CCCAACTAGT TCAGCTCAGC CAGGAAAGGG CAGGTCAGAT CTGGCTCAGC 960
AGGGGAGGCT GTGTCGGGGA GTGGTGCTGA CTCAGGGCCT GGTGAGTCAG GTGACAGCCA 1020
AGGACAGCTG TTGCCTGGGT GTTTTTAGAA AACTTTGGCT GCCAACCACT CTCTCATGGG 1080
TGCTTCTGCA CCTACTCAGA AGCAGGCAGA AAAAAGGAGG GCATCTTCTG TATAAGAAGC 1140
TCTGGGTGAG GGGTATTAAT ATCTGGCTCT ACTTATGTTG ATCCTTCCCA TGAAGTACCT 1200
AGAAAACGGA GCAGAAATTA ATTGAGAGGC TTCCAAATCC CTTCTGAATT CTCTGAAAAT 1260
CACTTATCTT TTCTGCTTAG CTCTTTTTAG GCACCTTGCC AGGTATCCAG CATAGAGGTT 1320
AAGAGAGCAG GCTCTGAAGT TAGGAGGGCC TGGGATCAAA ACCTAATTTC ATCATTTATA 1380
GTTGTATGAC TTAGATCAGA CTAAAAACAA 1410
|
