| Tag | Content |
|---|
EnhancerAtlas ID | HS018-12849 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr2:111750200-111752600 | SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
| | | 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 |
| GH02I110991 | chr2 | 111749325 | 111752589 |
| Enhancer Sequence | CTCCATGGGA CGAGGTAAGG CAGATGGAGC ATGGCAGGGA GAGGAGCCCT GAAAGGAAGT 60
GGCTTTGAAA GGGGGTTGTA CCTGGCTCTG CAGATAGCCC CATTCAGCTC TGGCTTGTCC 120
CTGCAAGGGT TGTCTCTCTT CCTCCTGCAT GGTAGCCTGC CACTGGGGCC CCTCCCACTC 180
TCATCAGCCT GTGGACCTTT AGGAGGTGGT GGTAGATGTC CAGGAAAGTC AAGATTTTGC 240
CTTGCACCCA ACGTGTTTTT CTACATTATG CTGTAAAATT TACAAATATT CAGCAAAGTT 300
GAAATAATTT TACAGGAAGC ATTTATGTAC AAACCATGGA GATTCTATCA ACCTATTACT 360
GTACCTGCTA TATCACTATC ATATCTATGG ATCTGTGTAT GGAACTCACC CATCCATTCA 420
CCTTCTCTTT TTGATCCATT TCAAAATAAA CTGTAGACAT CAGCACATTT CTAAATAATT 480
TAGCATGAGC GTCATTAACT ACAGTTACAT ATTTAGTTAT AGTTCTTCTT ATGTTGAATT 540
TACGTACAAT AAAATGCACA AATCTTAAGT GTACATTCAC TGAGTTTTGA CACATGCATA 600
AACCTATGTA ACCAAACTCA TATTAAGATA CAGATCATCA CTCCAGAAAG TTCTTTCATG 660
CCCCTTCTTG GACAATCTCA CTACGCAGAT ACAGCCACTC TTCTGATATT TTCCCACCAC 720
AGATTAGTTT TTCTATACTA GAACTTCACA TAAACAGAAC CAGGCAGTAT GTACTCTTTT 780
GTAGCTGCCT CGTGAAATTG GCATAATACT TTTTGACATT CACCCATGTT GTTGTGTGTA 840
TTAGTTTGTT TCTTTTCATT ATTGTAGTAT TTTACTTTAT GGATATAGTA GAATCATTCT 900
CTTATGGATG AATAGACACC TGGGATGTTT GCTGTTTCTC ACTTCTGTGA GTAGAACCGC 960
TATGAGCATT CTTGTATAAC CTTTTTTGTG AGCATATGTT TTTATTTCTC TTAGGCAATT 1020
AGTAGGAGTG AAACTGCTAG ATCATAGGGT ATGTGTTCAT TTATTTTTAT CAGAAACTGT 1080
GACAACATTT TGCAAAGAGA TTTCACCATT TTACACTCCC ATCAGCAAGC ATGAGAGTTC 1140
TGGTTTCTCC AGATCCTGGG CAACACTTGA TGTCAGTGTA CTTAATTGTA GTCATTCTGG 1200
TGGATGTATA ATGCTACCTC ACTATGGTTT CCGTTTGCAT TTCCCTGATG TCTAATGATA 1260
CTTATTTTAA TTTAATTTAA ACTTTATTTA AAAATAGAGT CATTTGGATC TTCTTGTAAA 1320
ATACACAGTT ACAAGGAGGT TGCCTTTAGC AATGTTTCTA TTTTTAAAGA AAGTCTGCAC 1380
ACTCTACTGC ACTGGGCAGG CTCCTAGACC TACATGACAT GTGACTCACA TGACTCAGCG 1440
AGTGGGTGAG ATCCCCTTCC TGCAGCACGT GCAGTTCACA ATCTCAGGTG GACAAACATG 1500
TTCTACAGTC TGAATTCCAG GGAAGCTAAT TTCCAATATC AGCCCCTGGA ATGACTAAAA 1560
CATACTTTTC AATAATATAT GAAAGCTTTT TACATCTTTC ATTAAATAGA CTGAGGCAGA 1620
AACCCAAACT TCTTAAAGCC CAGATTCAGA ATAAACATTG ACATCTTTTA AATGTCCCGG 1680
TAATTGGCAT GTAAATACTT TCCTCTTCCC TGTCTAAATG GAGGGTGATT ATTAATTCAG 1740
CACTTGGCAT CTCAAAAGCA CTGCGTCAAT TGCTTCTTAA CGTTTCTCTC GTGCCTTCTG 1800
ATTGAGCAAC AACAGCCACT TGGGTTTTTT TTTAGTTAAT ATGAATTTAA GTTATTTGAG 1860
TCTTGTAATA ACTTACTTCC TCAGGAAGTG GGGAAAGGGG AGGGCAAGAG GTGGCTGTGC 1920
TATGGGAAAC CCTAAGTGTG AATTAACCCT TCCCCTGGTT GTCTAGGTTA TCTAAAGGTT 1980
CATGGTGGGT CCATAAAATT GGCATGAAAT AGAGTTTCAT GATGAAAAGC TCACGAGCTT 2040
TTAATTGTGA ACTTGGTTGT TTTGAGTCTG TGCTTACCTC TCTTAACTCC TCTGTGCCTC 2100
AGTTTCCTCA TTTGCCAAAT GGGAAAGATG GGAATTGCTG CCTGCTGAAG AAAGCTACCA 2160
TCTCTGTAGC ACATCCTCCC CTGTGCTTGC ACACAGCCCT ATCACTTCCC TCCAGGGTGC 2220
CTCTTGCTTT AAATGCTGAT GTTCCCCAAC AAAACCTGAG CTTGACTGAG TTCTGCCTGT 2280
GTGACCTTGA GCAAGTTACC AAATCTTGCT AAGCCTCAGT TTCCTAAACT CTACATTGGA 2340
TAATTATAGT ATTCTAGAAT TATCGAGAAA ATTGAATAAT TCACAGCAGA TAATGAACAC 2400
|
| |
|
|
|
