EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS146-12382 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr6:11210960-11213510 
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr6:11210978-11210996GGAAGGAGGGAGGGATGG+6.94
FOXF2MA0030.1chr6:11212686-11212700TTTGTTTATCTTTA-6.02
PPARGMA0066.1chr6:11213004-11213024AGTTGGTCAGCATGACATAC-6.09
SOX10MA0442.2chr6:11212262-11212273TCCTTTGTTTT-6.32
Sox3MA0514.1chr6:11212263-11212273CCTTTGTTTT+6.02
TEAD1MA0090.2chr6:11211405-11211415ATGGAATGTG-6.02
TFAP2AMA0003.3chr6:11212887-11212898TGCCTCAGGCA+6.02
ZNF263MA0528.1chr6:11210987-11211008GAGGGATGGGGGGAGAGAGAG+6.07
ZNF263MA0528.1chr6:11210995-11211016GGGGGAGAGAGAGAGAGAGAG+6.3
ZNF263MA0528.1chr6:11210983-11211004GAGGGAGGGATGGGGGGAGAG+6.88
ZNF263MA0528.1chr6:11210960-11210981GGAGGAAGGGAGGGAGAGGGA+7.54
ZNF263MA0528.1chr6:11210979-11211000GAAGGAGGGAGGGATGGGGGG+7.92
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_00114chr6:11206173-11235315Adipose_Nuclei
SE_01650chr6:11209437-11217148Aorta
SE_02337chr6:11209467-11212265Astrocytes
SE_02337chr6:11212403-11214195Astrocytes
SE_20466chr6:11209500-11212542CD56
SE_23016chr6:11210253-11211987CD8_primiary
SE_23435chr6:11210898-11211848Colon_Crypt_1
SE_24670chr6:11210954-11211351Colon_Crypt_2
SE_25994chr6:11206468-11216792Duodenum_Smooth_Muscle
SE_29858chr6:11208642-11212468Fetal_Muscle
SE_29858chr6:11212497-11216549Fetal_Muscle
SE_32170chr6:11210946-11211835Gastric
SE_36359chr6:11212395-11213712HMEC
SE_37975chr6:11204960-11226988HUVEC
SE_41289chr6:11209401-11223624Left_Ventricle
SE_42296chr6:11210227-11221198Lung
SE_44826chr6:11210764-11211974NHLF
SE_44826chr6:11212092-11216756NHLF
SE_45752chr6:11205990-11214989Osteoblasts
SE_52869chr6:11210865-11212286Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr61121282411213214
Number: 1             
IDChromosomeStartEnd
GH06I011205chr61120603311225896
Enhancer Sequence
GGAGGAAGGG AGGGAGAGGG AAGGAGGGAG GGATGGGGGG AGAGAGAGAG AGAGAGAGAG 60
AGAGATAGAA AAGAGAAGTG AGGAAGGGAG TGAAAAGAAA GGAAGAGGCA ACCACACTCC 120
CATGGATGTG AACCACTGCT CTGGGGTACA TGGAGAGAGG CAGCCTAGAG ACCCAGGATC 180
AGGATACTGT GGAGAAGCCC TTGGTATTTG GCAGGGAAGG TGCCAGGGCC ACCCTCTTGC 240
CCTCCCCATC CTGGCCATGT CACTACCCCA GACCCTGACT GTGTGATGCT TTAGGCACGG 300
CCTACTCTTC AGCCCTGGCT GCAACTCCTG GAAGGGCTGG CACAGGTCAT TTTCAGAAGT 360
TGATTTCCTC CTGCAGGACT CATCTACCTT TTGCTAAACA GAAAATGTTC TACTGAGTGT 420
AGACTTAAAA AAAGCAAAAC AAAACATGGA ATGTGAGTGC CCGAGGGTCA CCCCAGCACC 480
CCAGCCCTTT GACATCAATC CAAGGGAAGA TGAGTCCGTA TCTCTGCCCT CTGGAAGGAC 540
GGGGAGCCAT GGGGAAAGCC TGCAGGGCAG TCCCAGCAGA TACAAGGGGA AGAAGTCTGA 600
AGGCTTAGGC TTCTCTGACT TGGAGCTGAA AAGGTTGGGT CTAAAAAGGA AAACACGCTA 660
CCTTCCTGCC AAAGTCAACT GTGATGAAAG TTTAGAGCCC ACCACCTCCC AGCCAAGCAT 720
TTCCTGCTCT GGCCTCCCCT TCTGCCTCAC ACTGGCTCAG ATGTGGGAGA GCTATTTTTA 780
AGGTGCAAAC AACCAGGACT AAGAATGAGT GAAGTTACTT ATTTATAGTT ACACCTTTCA 840
ACTGTTATTT TTCCCCTCTG GAGATAGAAG CCAGGTTTTG TTTTCCCTTT GAATCTACAA 900
TTCCTAGGAC AAGGAAGACT GAAAAGCCAC AAGTCAGTTT ATCACCTCTA GGCAGCATCG 960
TTGTCGTGGG CAGTACAAGT CTAAAAGCTG TGCACCACCC TTGAGGAATC CCTCTTAACG 1020
AACCTACGCT CAGTTCATGC CACACGCGTG CTCTTGAGAA GTATTTTGTA AAACATACTT 1080
TTTATATCAA AGGTGATTTA AAAATGCATT AGTGCTTTGT TGTTTAAAGG AATCTACCCA 1140
CACAGGGTCA GGGTCTGGGG TGGTGACATG GCCAGGATGG GGAGGGCAGG AGGGTGGCCC 1200
TGGCACCTCC CCAGCCAAAC ACTAAGGGCT CTCCACAGGG TCTCTAGGCT GCCTCTTTCC 1260
ATGTACCCAA AAATGCATTA GTGCTTTCAT TGTTTAAAGG AATCCTTTGT TTTTTCAACA 1320
GAGGATTCTA ATACATCAAA TAGATATTCC CTAATTTACA GAGGTTTGTA AAATCAGACT 1380
TCATATTAGA TTTACTTGGG GCAGGACACA TCTATAGTTA GTGTTCTAAG GGTCAACAAG 1440
CTCTTTCTGG TATGTAATTG CATCTTTCCT CTTGTAATTC AGGGATATCT TCTTATCCAG 1500
TTAAATTTGT TCATTCCTAA TACCAAACCT TGTAGGACCC ATTGGAATTT GCCAGCAAAT 1560
GAAAGAGAAA ATCCCTCCTT TGTGATGCTC ACATAAGCAT CACCTTGGTT GTGGGTGTTA 1620
CCCCCGATCA GTCCACTGAC ATTATTTTCC TGATAACACG TGTCCCTACC TAGCATTCTC 1680
TTGGTTGCTT CTGTCTCCCC CACGGCAATG TAAGCATCAC CAGGGCTTTG TTTATCTTTA 1740
ATTAATCACT GTATCACAAG CATCAAAAAT ATATTAGATG CTCAACATTC ATTGTTCAAT 1800
TAGTGAATTT CTATTGACCT CAAATTGCTA AAGTATTTGG GATTACACAG GGTGTTGCAG 1860
AGCTCCCCAC ACTGTATTTT TAAATTAATT CCTTCCTAAA TATCCAAGCT CCACTGTTTT 1920
CACCCACTGC CTCAGGCATT ATTATAAGAA TGACTTGAAG GACAGGAGGA TGGCTTCATT 1980
CCAATTCCAC TAGTATCTGT GCATTTTTAA ATGAGTCAAA CTAAGCTGAT AACTCTATAG 2040
AACGAGTTGG TCAGCATGAC ATACTCCCAG CTTCCTCACT CTCGCTACTT TGGGTGGGTT 2100
CCTTGTCCAG CCAGGCCACT GAGGTCATGA TTCAGCTTTT GGCCAAGGGA GGATCCTTGT 2160
TGCATCATCA GGCTTGTACG AGATTTGGTG TTTGTTCCAC TCAATGAAGA AACAGAAAAG 2220
ATAGGAAACG ATCTGAGCAC AGAGTGAAGG CTTAGAAGCT GATATATGAG AAAGATGGAG 2280
AGAAACAGTT TAATAACCCA TGTAACCCAG GATGACACAG GAACTTAGGA GGGCTGGAAA 2340
TCAACTGTAC TCAGCACATG GTAGTTCAAA GAAGTTTTGC TGAATGATGG ATGAATGGCA 2400
AAATCATGCA AACATGATGC CTGAGCTAAG GTATTGGTTA TATCTACTTC TTGGCAGCTT 2460
CAAGTTATTA ATTTGGGAAC ATTTCCAAAT GCTCCAAGTG TAATGGGAAA AAAAAATAAG 2520
TAGGAACAAA AATTTAGTTA GTCATTTACT 2550