| Tag | Content |
|---|
EnhancerAtlas ID | HS095-07569 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:89784030-89785460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr12:89784160-89784171 | GAAGATAAGAA | - | 6.02 | | PHOX2A | MA0713.1 | chr12:89784593-89784604 | TAATCCAATTA | + | 6.02 | | Phox2b | MA0681.1 | chr12:89784593-89784604 | TAATCCAATTA | + | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_25078 | chr12:89784165-89785524 | Colon_Crypt_3 | | SE_27644 | chr12:89782519-89785793 | Fetal_Intestine | | SE_28566 | chr12:89782048-89785987 | Fetal_Intestine_Large | | SE_35767 | chr12:89782928-89786699 | HepG2 | | SE_38298 | chr12:89782753-89785888 | HUVEC | | SE_41177 | chr12:89783038-89785367 | Left_Ventricle | | SE_48925 | chr12:89783907-89785560 | Right_Atrium | | SE_50215 | chr12:89783892-89785574 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I089388 | chr12 | 89782568 | 89786661 |
|
Enhancer Sequence | ACAACTCTGC TCATTTCCTC TTCCTGATGG TGCTGCTGTG ATTGCAGAAC TCAAGTAAGG 60
GCTTTTTACT ATATGAGAAT ACATGAGAAA TGATGCTCAA GTCATAATAA ATGTGAGATT 120
AAGGTCACTT GAAGATAAGA AGGTTGCAGC CTTAAGGAAA AACTTCAGTT GGCTTGGACC 180
TCTGCGGGGG CAGGTTTACT GTAGTTTGTG GAAATAACCC ACAGCTACTA CTGAAATATG 240
TGTAAGGATT TCAGACAGGA AATGAAGGAA ATGCTGCATT AAACTAAAAG CACTTTAGGA 300
TTTAAATAAG CCGAATATAG ATTCTCTGGT GAGAATTTGA TCAGGGCACT GCTGGCATTG 360
GCCCACCCTC TCATCTACAG TAGTGGAATT ACAGTCTGCC TATCAAGTCC AGAATACAAA 420
GTGCTTTCAG TCCTCTGACT ATCCTCTTTC CTCTTTTATT AATTCCATTT CTCATTAAAA 480
TCCCCTGTAC AATGTTCCAT GAGAGTGAGC TCAAGGCAGC TACTGACATT TCCCATAAAT 540
GATACGCCCA ATCTTCTTCC TACTAATCCA ATTAGTTCTA CTTCCTTCAA ACTTCATTCA 600
AAACTCAACT CATCTGATCT ATGCCTGATG ACCTTACAGT CATTCCTTGT CACTGTAAAC 660
CCTCAGCAGT TATTGTTGAC TGATTTGCTC ACTATGACCA TGTGTTTACT TGTGCCTGGC 720
ATTAGGCTTG GTGCTGGGGC TACACTGATG AGTAAACCCC AGTCACTGCC CTCATGGAGG 780
TCACAGTTCA CATGAAAAAA ACATCCTAAT AAACTGTGAT AAGGGCAATG GTCAAGATAG 840
GCATGCGGAA GTATGAGGAC AAGACATTCA TCCTCTGGGG TGTCAGAAGG CTTCCTGGAA 900
AAGCTGATGC CTGAGCTGGA TTTTCAAGTA GAGGAAGGTC GGGGAGATAT AGATGGTAGG 960
TAGTGTAATC CATGAACAGT TGAGATGGCC CTGTGTGCCA TGGTATGCTT GGGTGTATTC 1020
ATGACTTTCA CTTCATGAGA AGTTCCCTGT ATTTGGGTTC TTTTCCTACA ATTGAATTAT 1080
AAGCTCTTCC AGGAACCATA TTTTCTACTT ATTTTGCCTT CTTCCCCTTG GGTCTCTTAC 1140
AGTCCCCAGA GAGTTTTAAA GAGTTGTGTT TCACCATCCT GGGAAACACA CTGCTGACTC 1200
ACTGACCACC TCCAGGCCAC TCTGCCCACC GTGTGTTAAC AAGACTGTGT GGCCATGGAA 1260
AGATATGTAA GGCTGCAAGC CTTTTATCAG CTGTCAGGAT AGACCCAGGA AGACACACAG 1320
GTCTGACTCA AAGCACATAT ATACTGCCTA ATGGAAGAAA CCATCCAAAC CACTTACCCA 1380
GAAGTTCCAC AAGCCCATCA CATGCCATCC TTCCACTATT TCATATTCTT 1430
|
